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  • Organic Chemistry  (6,634)
  • Inorganic Chemistry  (5,245)
  • FLUID MECHANICS AND HEAT TRANSFER  (3,328)
  • GEOPHYSICS  (3,294)
  • 2015-2019  (33)
  • 1990-1994  (14,741)
  • 1950-1954  (3,727)
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  • 101
    ISSN: 0899-0042
    Keywords: chiral stationary phases ; resolution of enantiomers ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The determination of enantiomeric purity of (R)- and (S)-2-hydroxy-4-phenylbutyric acid by chiral HPLC is described. Good resolution has been obtained on covalently bonded L-hydroxyproline saturated with Cu(II) ions. The method makes possible the determination of enantiomeric purity in media containing growing cells. © 1994 Wiley-Liss, Inc.
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  • 102
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 6 (1994), S. 623-626 
    ISSN: 0899-0042
    Keywords: rat ovary microsomal aromatase ; enantiomers ; aminoglutethimide ; rogletimide ; cyclohexylaminoglutethimide ; stereochemical configurations ; aromatase inhibitors ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The in vitro aromatase activity in microsomal fractions from rat ovary and its inhibition by enantiomers of aminoglutethimide (AG), rogletimide (RG), and cyclohexylaminoglutethimide (ChAG) were studied by analysing the [3H]H2O released when [1β-3H]androstenedione was converted to estrone. Maximum velocity (Vmax) and the Michaelis-Menten constant (Km) of the microsomal aromatase enzyme were 17.40 ± 0.45 pmol/ml/mg protein/min and 1.02 ± 0.06 μM, respectively. The IC50s for the enantiomers were similar for (+)-R-AG and (-)-R-ChAG (0.86 ± 0.06 and 0.89 ± 0.15 μM, respectively). (+)S-ChA'G was most potent with IC50 of 0.075 ± 0.003 μM. The IC50s for (-)-S-AG, (+)-R-RG, and (-)-S-RG were in the same range (23.15 ± 2.74, 24.58 ± 2.46, and 24.43 ± 2.20 μM, respectively). © 1994 Wiley-Liss, Inc.
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  • 103
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 6 (1994), S. 649-653 
    ISSN: 0899-0042
    Keywords: organogels ; reversed micelles ; Aerosol-OT ; lipase ; 2-methylbutyric acid ; ethyl-2-methylbutyrate ; enantioselective reaction resolution ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chromobacterium viscosum lipase (c.v. lipase) was immobilized in microemulsion-based órganogels and successfully utilized for the enantioselective esterification of (+/-)-2-methylbutynic acid to preferentially form ethyl-(+)-2-methylbutyrate. The reaction time course and enantioselectivity obtained with the organogel - lipase system was compared and contrasted to that achieved in a reversed micellar solution system that contained lipase solubilized in its inner water core as well as that in which powdered lipases were directly dispersed in an organic solvent. The unique properties and potential benefits of the organogel system are discussed. © 1994 Wiley-Liss, Inc.
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  • 104
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 6 (1994), S. 665-669 
    ISSN: 0899-0042
    Keywords: circular dichroism ; amphotericin B ; self-association ; manomer/oligomer ; solvent effects ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Circular dichroism (CD) spectroscopy has been used to evaluate the ability of 21 different solvents to influence the aggregation state of amphotericin B. Using the relative donor/acceptor tendencies known for each solvent system, it was possible to deduce information as to the factors which goven the self-association of amphotericin B. It was concluded that in the absence of strong solvent interaction, amphotericin B prefers to self-associate into oligomeric species. This intrinsic driving force can be overcome through the use of solvents which function as strong electron pair donors, probably forming specific solvent - solute species. © 1994 Wiley-Liss, Inc.
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  • 105
    ISSN: 0899-0042
    Keywords: calcium channel blocker ; diastereomers ; chiral stationary phases ; liquid chromatography ; supercritical fluid chromatography ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The four optical isomers of a new calcium channel blocker LF 2.0254 (developed by Laboratoires Fournier) are resolved by chromatography using chiral stationary phases. Two methods are proposed: the first one involving two chiral stationary phases [(S)-N-(2-naphthyl)alanine, a Pirkle type CSP and Chiralcel OJ, a cellulose derived CSP] in the liquid chromatographic mode, the second one involving a single CSP (Chiralcel OJ) in the supercritical fluid chromatographic mode. © 1994 Wiley-Liss, Inc.
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  • 106
    ISSN: 0899-0042
    Keywords: chromatographic resolution of stereoisomers ; molecular modelling ; conformation ; κ-opiate receptor ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The four stereoisomers of the two peripherally selective κ-opioid agonists EMD 60 400 and EMD 61 753 were synthesized, tested for stereoisomeric purity, and examined for affinity to the κ opioid receptor. The relationships between the configuration of these molecules and their biological activity are discussed. © 1994 Wiley-Liss, Inc.
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  • 107
    ISSN: 0899-0042
    Keywords: benztropine ; histamine ; H1-receptors ; molecular modelling ; 4-methyl-diphenhydramine ; stereoselectivity ; synthesis ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of optically active analogues of the H1-antihistamine ebastine, with chiral center(s) at the benzhydryl and/or phenylbutyl part of the molecule, have been synthesized. Their in vitro antihistaminic and antimuscarinic activities were investigated, along with a molecular modelling study. It was found that introduction of the benzhydryl chiral center yielded significant stereoselectivity for both antihistaminic and antimuscarinic activities. The steric preferences of the benzhydryl chiral center for antihistaminic and antimuscarinic actions were mirror images of each other. The (-)-isomer of 4-methylebastine (6d) showed more than 10-fold higher in vitro antihistaminic potency than ebastine. Meanwhile the selectivity of 6d for histamine H1-receptors was also increased by more than 20 times in comparison with ebastine. The chirality at the phenylbutyl part of the molecule does not significantly alter the antihistaminic or antimuscarinic activity of the compounds although the (S)-isomers showed slightly but unanimously higher antihistaminic activity than the (R)-isomers. These results have been discussed with existing stereoselectivity data of antihistamines and an asymmetric pharmacophore model for H1-antagonists has been described. © 1994 Wiley-Liss, Inc.
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  • 108
    ISSN: 0899-0042
    Keywords: ketorolac ; nonsteroidal antiinflammatory drugs ; chiral drugs ; enantiomers ; protein binding ; human serum albumin ; enantioselectivity ; pharmacokinetics ; fatty acids ; oleic acid ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The protein binding of the enantiomers of the nonopiate analgesic, ketorolac, was investigated in vitro using human plasma and solutions of human serum albumin (HSA) at physiological pH and temperature. In order to detect the very low levels of unbound enantiomers in protein solutions, tritium-labelled rac-ketorolac was synthesised by regiospecific isotopic exchange of the parent drug with tritiated water as the isotope donor. Radio-chemical purification of this compound by reversed-phase HPLC followed by direct resolution using a chiral α1-acid glycoprotein (Chiral-AGP) HPLC column afforded labelled enantiomers of high specific activity. The in vitro use of (R)- and (S)-[3H4]ketorolac enabled reproducible radiometric detection of enantiomers in protein solution ultrafiltrate. The unbound fractions of (R)- and (S)-ketorolac [fu(R) and fu(S), respectively] were determined when drug was added to various plasma or albumin solutions as either the separate enantiomers or as the racemate. Over an enantiomeric plasma concentration range of 2.0 - 15.0 μg/ml, fu(S) (mean range: 1.572 - 1.795%) was more than 2-fold greater (P 〈 0.001) than fu(R) (mean range: 0.565 - 0.674%). Both fu(R) and fu(S) were constant over this concentration range, and each was unaffected by the presence of the corresponding antipode (P 〉 0.05). At a concentration of 2.0 μg/ml in 40.0 g/liter fatty acid-free HSA, fu(R) and fu(S) were approximately 0.5 and 1.1%, respectively, and both values declined with increasing concentrations of the long chain fatty acid, oleic acid. We have previously shown that the pharmacokinetics of ketorolac in humans are markedly enantioselective and suggest in this report that these differences are largely the result of substantial differences in the protein binding of ketorolac enantiomers. These findings stress the importance of monitoring the unbound concentrations of the enantiomers of chiral drugs if correct interpretations are to be made of enantioselective pharmacokinetic data. © 1994 Wiley-Liss, Inc.
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  • 109
    ISSN: 0899-0042
    Keywords: chiral cyclic hemiketal derivatives NMR data ; crystal structure elucidation ; high-performance liquid chromatography (HPLC) ; quinine salt resolution of rac-endo-1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2-carboxylic acid ; preparative resolution of rac-warfarin and rac-p-chlorowarfarin ; reaction mechanism ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of rac-warfarin, (-)-(1S,2R,4R)-endo-1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-ene-2- carboxylic acid [(-)-HCA] and carbodiimide reagents gave two noncyclic ketonic diastereoisomeric derivatives whereas rac-warfarin and (-)-HCA acid chloride with 4-(dimethylamino)pyridine gave four cyclic hemiketal diastereoisomeric ester derivatives. The structure and stereochemistry of diastereoisomeric esters prepared from warfarin and p-chlorowarfarin were determined from 1H- and 13C-NMR spectra, mass spectra, and hydrolysis to warfarin and p-chlorowarfarin enantiomers. The structure and stereochemistry of one of the cyclic hemiketal diastereoisomeric derivatives of warfarin are supported by an X-ray crystallographic determination. Mechanisms for the formation of all products are proposed. © 1994 Wiley-Liss, Inc.
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  • 110
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 6 (1994), S. 691-691 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 111
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 6 (1994), S. 658-664 
    ISSN: 0899-0042
    Keywords: host-guest cyclodextrin complexes ; asymmetric induction ; solid-state reaction ; substituent effect ; steric restrictions ; hydrophobic interactions ; hydrogen bonding ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of substituent groups on asymmetric induction by β-cyclodextrin (β-CD) was investigated in the reduction of a series of o-, m-, and p-substituted acetophenones (X = H, Br, Cl, CH3, NO2, OCH3) with aqueous NaBH4. The inclusion of the ketones studied in β-CD led to water-insoluble compounds so that the reaction proceeded in the solid state. The substitutions resulted generally in higher enantioselectivities than that obtained for acetophenone indicating stronger host - guest interactions. Acetophenone and its m- and p-derivatives gave preponderantly the (-)-alcohol while the prevailing enantiomer was the (+)-alcohol in the case of the o-derivatives. The enantioface selectivity was found to be mainly governed by steric demands imposed by the size and the shape of the β-CD cavity in the case of the o-substituted acetophenones and by hydrophobic interactions in the case of the m-derivatives. A more complicated situation arose from the asymmetic reduction of p-derivatives where a combination of these factors with hydrogen bonding of the carbonyl group to the hydroxyls of β-CD are responsible for the enantioselectivity. © 1994 Wiley-Liss, Inc.
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  • 112
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 6 (1994), S. ii 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 113
    ISSN: 0899-0042
    Keywords: antiarrhythmic agents ; mbe-lactole ; rsp-cyclodextrine ; preparation of enantiomers ; GE 68 ; pharmacodynamic activity ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An improved synthesis of the enantiomers of the new benzofurane-type antiarrhythmic compound 1 is described, which makes use of the enantiomerically pure mbe-lactol. Thus, acylation of the benzofurane 4 with acetic anhydride and subsequent bromination gave the bromoacetyl-derivative 6, which, after reduction with LiAlH4, was protected with mbe-lactol to give a mixture of the diastereomers 8A and 8b. After separation via column chromatography assignment of absolute configuration was carried out using a well-established NMR- method. Reaction with propylamine and cleavage of the protective group gave (R)-1 and (S)-1, respectively. Enantiomeric purity was confirmed using a direct HPLC method with rsp-cyclodextrine as stationary phase. Pharmacological investigations on isolated guinea pig heart muscle preparations showed that GE 68 and its two enantiomers did not significantly differ from each other with regard to their negative inotropic, negative chronotropic, and lack of β-adrenoceptor blocking action. In contrast, the reference drug propafenone was equally potent in its negative inotropic and chronotropic activity as GE 68, but additionally showed a weak β-adrenoceptor blocking activity. © 1994 Wiley-Liss, Inc.
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  • 114
    ISSN: 0899-0042
    Keywords: hydroxychloroquine ; enantiomers ; stereoselectivity ; distribution ; interconversion ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydroxychloroquine (HCQ) stereoselective distribution was investigated in rabbits after 20 mg/kg po of racemic-HCQ (rac-HCQ) and 20 mg/kg po of each enantiomer, 97% pure (-)-(R)-HCQ and 99% pure (+)-(S)-HCQ. Concentrations were 4 to 6 times higher in whole blood than in plasma. Melanin did not affect plasma and whole blood levels since concentrations did not differ between pigmented and nonpigmented animals. After single and multiple doses of the separate enantiomers, only 5-10% of the antipode could be measured, in blood or plasma. Therefore, there was no significant interconversion from one enantiomer into the other. Following rac-HCQ, plasma (+)-(S)-levels always surpassed (-)-(R)-ones while in whole blood, (-)-(R)-HCQ concentrations were always the highest. When the enantiomers were administered separately, blood concentrations achieved after (-)-(R)-HCQ were higher, especially after multiple doses. These observations suggest that (-)-(R)-HCQ is preferentially concentrated by cellular components of blood. This enantioselective distribution of HCQ could be secondary to a stereoselective protein binding to plasma proteins, although a more specific binding of (-)-(R)-HCQ to blood cells cannot be ruled out. Since in whole blood (-)-(R)-HCQ is retained in cellular components, metabolism would favour the more available (+)-(S)-enantiomer. © 1994 Wiley-Liss, Inc.
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  • 115
    Electronic Resource
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    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 6 (1994) 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 116
    ISSN: 0899-0042
    Keywords: rat ; cytochrome P-450 ; toltrazuril ; sulfoxide ; sulfone ; pharmacokinetics ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pharmacokinetics of the antiparasitic drug toltrazuril (1-methyl-3-[3-methyl-4-[4-[trifluoromethyl]thio]phenoxy]phenyl-1,3,5- triazine-2,4,6(1H,3H,5H)-trione) were studied in the rat following pretreatment with 3-methylcholanthrene, an inducer of rat liver cytochrome P-450 1A. The induction markedly modified the pharmacokinetics of the compound, leading to a decrease in the AUC value for toltrazuril sulfoxide. The results were explained on the basis of previous results from our laboratory relating to the product enantioselectivity of the formation of the sulfoxide and the substrate enantioselectivity of the subsequent formation of the sulfone. © 1994 Wiley-Liss, Inc.
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  • 117
    ISSN: 0899-0042
    Keywords: antihistaminic ; antimuscarinic ; mequitazine enantiomers ; dextromequitamium iodide ; chiral separation ; absolute configuration ; conformational analysis ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The enantiomers of 1-methyl-3-(10H-phenothiazine-10-ylmethyl)-1-azoniabicyclo[2,2,2]octane iodide (1) were prepared by chiral chromatographic resolution of the precursor mequitazine (2). The (+)-(S)-enantiomer 1b is 10-fold more potent than (-)-(R)-enantiomer 1a as a histamine antagonist, while the two enantiomers show the same antimuscarinic activity in vitro. The absolute configuration of the more active dextrorotatory isomer has been determined by X-ray analysis. Conformational analysis and molecular modeling suggest that the (+)-(S)-enantiomer can adopt a conformation similar to that attributed to the receptor binding conformers of classical antihistamines. © 1994 Wiley-Liss, Inc.
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  • 118
    ISSN: 0899-0042
    Keywords: dialkylaminoalkylnaphthalenes ; optical resolution ; crystallography ; absolute configuration ; analgesic activity ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The alkylaminoalkylnaphthalene 3 shows interesting opioid-like analgesic properties, μ-selective ligand competition, and enkephalin hydrolyzing enzyme inhibition. 3 possesses two chiral centers and can exist as two racemic pairs and four diastereomers. Since the binding of opioids with the receptor is stereoselective, it was important to have the two racemic pairs as well as the four diastereomers. In this paper the synthesis of the (1R,2R/1S,2S)- and (1R,2S/1S,2R)-racemates and the (1R,2R)- and (1S,2S)-enantiomers of the 1-ethyl-1-hydroxy-1-[2-(6-hydroxynaphthyl)]-2-methyl-3-dimethylaminopropane 3 is considered and the determination of absolute configuration is described. The (1R,2R/1S,2S)-3 and (1R,2S/1S,2R)-3 racemates and the (1R,2R)-3 and (1S,2S)-3 enantiomers were prepared by reaction of the racemic and optically active 1-dimethylamino-2-methylpentan-3-one 2, respectively, with the lithiation product obtained from 2-bromo-6-tetrahydropyranyloxynaphthalene and acidic hydrolysis. The optical resolution of aminoketone 2 was carried out via fractional crystallization of salts (+)- and (-)-dibenzoyltartrates. The configuration of the optically active compounds was determined by X-ray analysis of a crystal of (+)-(1R,2R)-3 · HCl · H2O. Preliminary pharmachological tests showed that (+)-(1R,2R)-3 enantiomer is able to induce opioid-like analgesia with a relative potency 2.5 times that of (1R,2R/1S,2S)-3 and about 4 times that of morphine. © 1994 Wiley-Liss, Inc.
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  • 119
    ISSN: 0899-0042
    Keywords: 2-, 3-, and 4-alkyl-branched acids ; enantioselective analysis ; sensory evaluation ; heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrin ; octakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-γ-cyclodextrin ; Chamaemelum nobile (L.) Allioni ; Parmesan cheese ; red meat flavour ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enantioselective GC analysis of 4-ethyloctanoic and 4-methylheptanoic acid, using heptakis(2,3-di-O-methyl-6-O-tert-butyldimethylsilyl)-β-cyclodextrin as the chiral stationary phase, is described and the sensory properties of several 4-alkyl-branched acids, using gas chromatography-olfactometry (GC-O) equipment and octakis(2,3-di-O-methyl-6-tert-butyldimethylsilyl)-γ-cyclodextrin as the stationary phase, are evaluated. The chirospecific analysis of various 2-, 3-, and 4-alkyl-branched acids from commercially available Roman chamomile (Chamaemelum nobile (L.) Allioni), Parmesan cheese, and subcutaneous mutton adipose tissue, using either GC-GC (MDGC) or GC-MS analytical methods, is described. © 1994 Wiley-Liss, Inc.
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  • 120
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    Chirality 6 (1994) 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 121
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    Chirality 6 (1994), S. 72-75 
    ISSN: 0899-0042
    Keywords: chirality ; racemate ; enantiomers ; regulation ; review ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rapid development of stereospecific analytical, synthetic, and preparative methods has profoundly changed the prospects for development and application of chiral medicinal products. This has induced regulatory agencies, e.g., in Canada, the EEC, Japan, and the United States, to prepare guidance on this subject. The present draft documents are discussed, with emphasis on the two most important cases: (1) New racemates: How many extra requirements are justified? (2) Development of a single enantiomer from an approved racemate: how few are acceptable? At the moment the opportunities for early harmonisation are favourable and the formulation of one international guidance document seems feasible. © 1994 Wiley-Liss, Inc.
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  • 122
    ISSN: 0899-0042
    Keywords: pargyline N-oxide ; chiral nitrogen centre ; flavin-containing monooxygenase ; chiral stationary phase ; high-performance liquid chromatography ; Chiralcel OD ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The monoamine oxidase inhibitor pargyline (N-benzyl-N-methyl-2-propynylamine) is known to undergo extensive in vitro microsomal N-oxidation, thought to be mediated predominantly by the flavin-containing monooxygenase (FMO) enzyme system. Formation of the pargyline N-oxide (PNO) metabolite creates a chiral nitrogen centre and thus asymmetric oxidation is possible. This study describes a reverse-phase high-performance liquid chromatographic (HPLC) method for the quantitation of PNO and a chiral-phase HPLC method for the determination of the enantiomeric ratio of PNO. In vitro microsomal N-oxidation of pargyline was found to be highly steroselective in a number of species, with the (+)-enantiomer being formed preferentially. This metabolic transformation was stereospecific when purified porcine hepatic FMO was used as the enzyme source. © 1994 Wiley-Liss, Inc.
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  • 123
    ISSN: 0899-0042
    Keywords: cellulose ; phenylcarbamate ; 3,5-dimethylphenylcarbamate ; resolution 2.5 μm silica ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of particle size and pore size of the aminopropylated silica support for cellulose tris(phenylcarbamate) and tris(3,5-dimethylphenylcarbamate) chiral HPLC phases was investigated. It was necessary to reduce phase loading below 20% w/w as pore size and particle size were reduced, but high efficiency columns could be prepared at a 15% w/w loading on 5 and 2.5 μm supports with 120-Å-diameter pores. The 2.5 μm phase permits the use of relatively high flow rates and very efficient enantioselective separations of a range of chiral compounds could be achieved in less than 3 min. © 1994 Wiley-Liss, Inc.
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  • 124
    ISSN: 0899-0042
    Keywords: Horeau's method ; configuration of secondary alcohols ; enantioselective gas chromatography ; 2-phenylbutyric acid ; cyclodextrin derivative ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of optically active secondary alcohols with excess of racemic 2-phenylbutyric acid anhydride in pyridine proceeds at different rates to the diastereoisomeric esters (kinetic partial resolution). According to Horeau the (unknown) absolute configuration of the alcohol can be derived from the optical rotation of the remaining excess of 2-phenylbutyric acid in the reaction mixture. Measuring the optical rotation may be very difficult in cases of small absolute rotation values and may be inaccurate due to the necessity to completely remove all chiral impurities. The application of Horeau's method is greatly facilitated by gas chromatographic determination of the enantiomeric ratio of the remaining 2-phenylbutyric acid after methylation using a short capillary column with heptakis(2,6-di-O-methyl-3-O-pentyl)-β-cyclodextrin as a chiral stationary phase. Baseline resolution of the enantiomers is achieved after approximately 10 min of retention time. Due to the high selectivity of capillary gas chromatography the probability of impurities in the mixture to interfere with the measurement of the enantiomeric ratio is extremely low. © 1994 Wiley-Liss, Inc.
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  • 125
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    Chirality 6 (1994), S. 161-164 
    ISSN: 0899-0042
    Keywords: homochiral amines ; N,N-ditosylimides ; azides ; inversion of configuration ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: More effective use of optical resolution processes can be obtained by increasing the overall yields after development of methods for inversion of the chiral centre of the unwanted isomer. The configuration of some optically active amines can be inverted in a three-step synthesis via the N,N-ditosylimides and a subsequent nucleophilic substitution by the azide ion. The azide product is reduced by hydrogenolysis. Low stereoselectivity caused by racemization to some extent was at first observed for the inversion of the benzylic substrate, (S)-α-methylbenzylamine (5a). However, modified reaction conditions allowed increased stereoselectivity, a more rapid and almost complete inversion of this substate as well. © 1994 Wiley-Liss, Inc.
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  • 126
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    Chirality 6 (1994) 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 127
    ISSN: 0899-0042
    Keywords: atenolol ; enantiomers ; pharmacokinetics ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The purpose of this study was to describe the pharmacokinetics of and heart rate and blood pressure responses to (S)-atenolol (SATN) and (R)-atenolol (RATN) after oral administration of (S)-atenolol and (R,S)-atenolol (Tenormin™) in man. Eight male subjects were given single oral doses of 50 mg of SATN as a single enantiomer formulation (SEF) and 100 mg of Tenormin™ (TMN) using a randomized, double-blind, 2-period, complete crossover study design. Subjects performed exercise tolerance tests (Bruce Protocol) before and 2, 4, 6, 8, 12, and 24 h after drug administration. Plasma samples were obtained 2 min before and 30 min, 1, 1.5, 2, 3, 4, 5, 6, 8, 10, 12, 16, and 24 h after dosing. Urine was collected for the first 48 h after dosing. Plasma and urine samples were analyzed for SATN and RATN by an enantioselective HPLC method. SEF and Tenormin™ attenuated exercise-induced increases in heart rate and systolic blood pressure. Mean changes in exercise heart rates 4 h after dosing were -38 ± 3 bpm and -37 ± 3 bpm for SEF and TMN, respectively, P = 0.792. Mean changes in exercise systolic blood pressure were -42 ± 12 mm Hg and -55 ± 14 mm Hg for SEF and TMN, respectively, P = 0.484. Mean area under the plasma level time curve (AUC0-24) and mean Cmax for SATN for SEF were significantly lower than for SATN after TMN. Mean SATN AUCs0-24 were 1867 ± 261 and 2543 ± 223 ng · h/ml (P = 0.005) and mean Cmaxs were 225 ± 29 and 333 ± 30 ng/ml, for SEF and TMN, respectively (P = 0.011). Mean Tmax for SATN occurred significantly earlier after SEF than after TMN (2.9 ± 0.3 and 3.3 ± 0.3 h, P = 0.028). The amount of SATN excreted in urine was significantly lower after SEF than after TMN (18.7 ± 2.7 and 24.2 ± 2.0 mg, P = 0.017). AUC, Cmax, and amount excreted in urine (Au) were significantly higher for RATN than SATN after TMN. Mean AUCs, Cmaxs, and Aus for RATN compared to SATN were 2806 ± 239 vs 2543 ± 223 ng ± h/ml (P 〈 0.0001), 360 ± 31 vs 333 ± 30 ng/ml (P 〈 0.0001), and 25 ± 2.1 vs 24 ± 2 mg (P = 0.004), respectively. SEF and TMN are equieffective in attenuating exercise-induced increases in heart rate and systolic blood pressure. The SEF has lower bioavailability compared to TMN and RATN plasma levels are higher than SATN after TMN administration. © 1994 Wiley-Liss, Inc.
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  • 128
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An enantioselective assay has been developed for the determination of the enantiomers of ketorolac and its metabolite p-hydroxyketorolac in plasma and urine. The analytical method utilizes a coupled achiral-chiral HPLC system where the initial separation of ketorolac from p-hydroxyketorolac and matrix interferences was achieved on a C18-stationary phase and the enantioselective separations of the two target solutes were accomplished on a human serum albumin-based chiral stationary phase. The two columns were attached in sequence and the assay was carried out without the necessity of column-switching techniques. The method has been validated for use in pharmacokinetic and metabolic studies and represents the initial report of the determination of ketorolac and p-hydroxyketorolac enantiomers in urine. The results of the study indicate that after the administration of racemic ketorolac there was an enantioselective distribution of ketorolac enantiomers in plasma [(R)-ketorolac: (S)-ketorolac = 3.89 ± 0.93 (n = 6) and urine (R)-ketorolac: (S)-ketorolac = 1.26 ± 0.09 (n = 7)]. The mean ratio of the p-hydroxyketorolac enantiomers was 1.77 ± 0.46 (n = 7). Both ketorolac and p-hydroxyketorolac are glucuronized in the acyl carboxyl moiety and the results of this study indicate that this process is not enantiospecific. © 1994 Wiley-Liss, Inc.
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  • 129
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    Chirality 6 (1994), S. 321-328 
    ISSN: 0899-0042
    Keywords: oxazepam ; 3-O-acyloxazepam ; racemization ; kinetics ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enantiomers of 3-O-acyloxazepam (oxazepam 3-acetate; OXA) underwent base-catalyzed hydrolysis and racemization. Kinetics of reaction products formed from an OXA enantiomer in buffered and unbuffered alkaline solutions were analyzed by chiral stationary phase high-performance liquid chromatography. Racemization occurred with varying rates in aqueous solutions with pH ranging from 7.5 to 14. Racemization mechanism was studied by the dependence of rates of hydrolysis and racemization on temperature and pH. Mass spectral analysis of racemization products derived from an OXA enantiomer in a deuterated solvent indicated that racemization was accompanied by a proton exchange with the solvent. The results indicated that a base-catalyzed keto-enol tautomerism between the C2-carbonyl group and the C3 carbon was responsible for the observed racemization. © 1994 Wiley-Liss, Inc.This article is a US Goverment work and, as such, is in the public domain in the United States of America.
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  • 130
    ISSN: 0899-0042
    Keywords: enantioselective tissue sequestration ; hydroxychloroquine stereoisomers ; cornea ; iris ; retina ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The disposition of the enantiomers of hydroxychloroquine (HCQ) and its major metabolites in ocular tissues of rabbits has been studied. Both albino, New Zealand White (NZW), and pigmented animals were administered daily oral doses of rac-HCQ, (S)-HCQ or (R)-HCQ (20 mg/kg) over 1, 6, or 8 day periods or for 8 days followed by a 7-day washout period. At the end of the study periods, plasma and whole blood samples were collected and the rabbits were sacrificed. The eyes were collected, the aqueous humor removed with a syringe, and the eyes separated into the cornea, lens, vitreous body, iris, choroid-retina, sclera, and conjunctiva. The concentrations of (R)-HCQ, (S)-HCQ, and their respective metabolites were determined using a validated enantioselective liquid chromatographic assay. The data from these studies indicate that HCQ accumulated in both pigmented and nonpigmented ocular tissues. In the pigmented tissues, HCQ and its metabolites were bound to melanin and the binding was not enantiospecific. In the nonpigmented tissues and in the iris and retina-choroid of the NZW rabbits, the accumulation appeared to be the result of a reversible and enantioselective binding of HCQ and its metabolites to an unidentified biopolymer present in these ocular tissues. © 1994 Wiley-liss, Inc.
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  • 131
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    Chirality 6 (1994), S. 378-381 
    ISSN: 0899-0042
    Keywords: piperidine-2,6-diones enantiomers ; chiral recognition mechanism(s) ; enantioselective elution order and chirality ; cellulose-based chiral stationary phase ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The enantioselectivity and enantiomeric separation of five racemic piperidine-2,6-dione compounds, on the cellulose tris(3,5-dimethylphenyl carbamate) chiral stationary phase Chiralcel OD-CSP were investigated under the same chromatographic conditions. This class of drugs includes glutethimide, aminoglutethimide, cyclohexylaminoglutethimide, pyridoglutethimide, and phenglutarimide. The results revealed that chiral recognition and the binding sites of these drugs on the Chiralcel OD column are similar, regardless of the absolute configuration of the individual enantiomers. A possible chiral recognition mechanism(s) for this class of drugs and the CSP is presented. © 1994 Wiley-Liss, Inc.
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  • 132
    ISSN: 0899-0042
    Keywords: econazole ; 3-(4-aminophenyl)pyrrolidine-2,5-diones ; aromatase inhibitors ; antifungals ; drug registration ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The enantiomers of the aromatase inhibitors 3-(4-aminophenyl)-pyrrolidine-2,5-dione (WSP-3, II), its N-pentyl derivative (III), and the antifungal econazole (IV), all possessing a benzylic proton at the chiral centre, are rapidly racemised in vitro in phosphate buffer (0.01 M) at pH 7.4 and 23°C with t½ values of 7, 6, and 5 h respectively. In vivo studies in rats show that (+)-econazole is racemised after intraperitoneal injection with t½ = 1.24h. The enantiomers of the antifungal 1-[(benzofuran-2-yl)-4-chlorophenylmethyl] imidazole (V) were stable at pH 7.4, attributable to steric hindrance to carbanion formation in the racemisation step. © 1994 Wiley-Liss, Inc.
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  • 133
    ISSN: 0899-0042
    Keywords: atenolol ; nitrile formation ; stability ; chromatography ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemical stability of the acetamido moiety of the β-blocker atenolol toward possible dehydration causing a nitrile formation during an acid-catalyzed chiral derivatization procedure with O,O′-(R,R)-diacylated tartaric acid anhydrides was elucidated. All the necessary reference compounds including the oxazolidine-2-one derivatives of the respective aminopropanols were synthesized, their structures confirmed by various spectroscopic methods, and chromatographically compared using HPLC and GC-MS. In the course of this work it was shown that the acetamido moiety of atenolol is quite stable toward dehydrating agents but shows a significant thermolability, e.g., in the injection system of a GC, which leads to the dehydrated form of atenolol namely, “nitriloatenolol.” © 1994 Wiley-Liss, Inc.
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  • 134
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    Chirality 6 (1994), S. 681-684 
    ISSN: 0899-0042
    Keywords: sharpless asymmetric epoxidation ; detailed synthesis ; enantiomeric separations; diastereomeric separations ; cis- and trans-epoxy alcohols ; cis- and trans-allylic alcohols ; homoallylic alcohol ; chiral HPLC ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The detailed synthesis of (2R,3R)-3-benzylglycidol by the Sharpless asymmetric epoxidation route is described. The enantiomeric purity determination of this compound is complicated by the presence of small quantities of the diastereometric (2R,3S)-3-benzylglycidol from the asymmetric epoxidation of the cis-allylic alcohol, and the unreacted allylic alcohols that are not removed in the product isolation steps. We have developed a direct chiral HPLC method that can resolve all these components for the precise determination of enantiomeric excesses of chiral 3-benzylglycidols. © 1994 Wiley-Liss, Inc.
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  • 135
    ISSN: 0899-0042
    Keywords: blood pressure ; renal vasodilation ; dopamine agonists ; renal function ; renal blood flow ; diuresis ; renin-angiotensin-aldosterone system ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: SK&F 87516 is a potent DA1 receptor agonist with demonstrated renal vasodilator activity. SK&F 87516 is the 6-fluoro analog of another DA1 agonist/renal vasodilator agent, fenoldopam. SK&F 87516 is a racemic mixture of two enantiomers, SK&F(R)-87516 and SK&F(S)-87516, and like fenoldopam, the (R)-enantiomer is responsible for the biological activities of the racemate. SK&F(R)-87516 is diuretic in spontaneously hypertensive rats and in dogs, whereas its enantiomer, SK&F(S)-87516 is inactive. SK&F(R)-87516 increases glomerular filtration rate, an effect which may account, in part, for its diuretic activity. Unlike fenoldopam, SK&F(R)-87516 is not associated with acute hypotensive activity, tachycardia, or stimulation of the renin-angiotensin-aldosterone system. The activity differences between SK&F(R)-87516 and fenoldopam are not related to differences in DA1 agonist potency. The activity differences may be due to the differing effects of fluorine and chlorine on the electron distribution in the catechol ring, resulting in an enhanced effect of SK&F(R)-87516 at α2-adrenoceptors. © 1994 Wiley-Liss, Inc.
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  • 136
    ISSN: 0899-0042
    Keywords: chiral inversion ; oxindanac ; dogs ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The nonsteroidal antiinflammatory drug oxindanac exists as two enantiomers, with most of its pharmacological activity residing in the (S)-isomer. The behavior of its enantiomers was investigated in dogs. Bidirectional inversion occurred in heparinised plasma and blood, with a ratio of enantiomers [S:R] of 7.3:1 being achieved at equilibrium after incubation for 24 h at 37°C. There was no detectable inversion of either isomer in plasma incubated at 4°C for up to 8 h or in aqueous solution at 37°C for up to 36 h. Bidirectional inversion also occurred in vivo, with a ratio of plasma AUC (0 ∞)s [S:R] of 8.1:1. The ratio of enantiomers reached equilibrium within 2 hr following (S)- or rac-oxindanac, and within 8 h following (R)-oxindanac. Elimination t½s of the isomers were the same (R, 12.1 h, S, 13.3 h). There were no differences in the ratio of enantiomers following oral or intravenous application, suggesting that a systemic site for inversion was predominant. Although concentrations of the respective isomers were similar at equilibrium following administration of either (R)-, (S)-, or rac-oxindanac, AUC (0 ∞)s differed due to the delay in reaching equilibrium. The extent of inversion to the (S)-isomer was 100, 73.2, and 60.7% after administration of (S)-, rac-, and (R)-oxindanac, respectively. Although pharmacological activity might be equivalent at equilibrium following administration of either (R)-, (S)-, or rac-oxindanac; efficacy at early time points should be superior in the order (S) 〉 racemate 〉 (R). In conclusion both enantiomers of oxindanac undergo conversion to their respective antipodes in dogs, although the inversion of R to S is more efficient than that of S to R. This bidirectional inversion occurred in vivo, and in vitro in plasma and blood. © 1994 Wiley-Liss, Inc.
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  • 137
    ISSN: 0899-0042
    Keywords: timolol maleate ; quantitation of enantiomers by HPLC ; quantitation of enantiomers by NMR ; optical purity ; chiral separation ; cellulose tris-3,5-dimethylphenylcarbamate (Chiracel OD-H) ; chiral solvating agents ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: HPLC and 1H-NMR methods for the quantitation of the (R)-enantiomer in (-)-(S)-timolol maleate were developed and validated. The HPLC method requires a 25 cm × 4.6 mm 5 μm Chiracel OD-H (cellulose tris-3,5-dimethylphenylcarbamate) column, a mobile phase of 0.2% (v/v) diethylamine and 4% (v/v) isopropanol in hexane at a flow rate of 1 ml/min and UV detection at 297 nm. A system suitability test was devised to verify the separation of the (R)- and (S)-enantiomers of timolol from other drug-related impurities. The NMR method requires the use of a high-field NMR spectrometer (〉360 MHz) and a chiral solvating agent, (-)-(R)-2,2,2-trifluoro-1-(9-anthrylethanol) (R-TFAE). The limits of quantitation were 0.05% and 0.2% (m/m) for HPLC and NMR, respectively. The methods were applied to the determination of the (R)-enantiomer in eight lots of raw material. The results for the two methods were in very good agreement, with results ranging from 0.1 to 4.1% (m/m) by HPLC and none detected to 4.3% (m/m) by NMR. The USP method for specific rotation was found to be unsuitable for detecting the presence of low levels of the (R)-enantiomer in (-)-(S)-timolol maleate. © 1994 Wiley-Liss, Inc.
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  • 138
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    Chirality 6 (1994), S. 492-495 
    ISSN: 0899-0042
    Keywords: enantiomers ; methadone ; pharmacokinetics ; beagle dog ; iv administration ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pharmacokinetics of methadone were studied in beagle dogs (n = 4) following intravenous administration of the racemate (0.5 mg/kg) and of the individual (R)-(0.25 mg/kg) and (S)-enantiomers (0.25 mg/kg) using a stereospecific HPLC assay. There was no significant difference between the pharmacokinetic parameters of (R)-methadone and (S)-methadone following administration of the individual enantiomers. Stereoselective differences were evident following administration of the racemate (P values for differences in AUC and CL were 0.001 and 0.046, respectively) and the clearance of the (S)-enantiomer was increased when administered as part of the racemate (316 ± 81 vs 487 ± 128 ml/min, P = 0.04). The data suggest that stereoselective disposition including potential enantiomer-enantiomer interactions should be considered in pharmacokinetic-pharmacodynamic studies of (R,S)-methadone. © 1994 Wiley-Liss, Inc.
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  • 139
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    Chirality 6 (1994) 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 140
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    Chirality 6 (1994), S. 531-536 
    ISSN: 0899-0042
    Keywords: (R)- ; (S)- ; (R, S)-amlodipine ; pharmacokinetics ; oral dosage ; human study ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Plasma concentrations of (R)- and (S)-amlodipine were measured after single oral administrations to 18 healthy volunteers of 20 mg amlodipine racemate. The contribution of the pharmacologically active (S)-enantiomer to the concentrations of total amlodipine (sum of enantiomers) was significantly higher than that of the inactive (R)-enantiomer, with mean values of 47% R to 53% S for the Cmax and 41% R to 59% S for the AUC (range between 24% R:76% S and 50% R:50% S). The oral clearance of the active (S)-form was subject to much less intersubject variation (25% CV) than that of the inactive (R)-form (52% CV). (R)-Amlodipine was more rapidly eliminated from plasma than (S)-amlodipine, with mean terminal half-lives of 34.9 h (R) and 49.6 h (S). The terminal half-lives of total amlodipine (mean 44.2 h) were strongly correlated with - and thus highly predictive for - the half-lives of the (S)-enantiomer. It is proposed that the observed enantioselectivity of oral amlodipine is due to differences in the systemic blood clearance of the enantiomers. © 1994 Wiley-Liss, Inc.
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  • 141
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    Chirality 6 (1994), S. 549-554 
    ISSN: 0899-0042
    Keywords: high-performance liquid chromatography ; chiral stationary phase ; optical isomer resolution ; ergot alkaloids ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new covalently-bonded, silica-based stationary phase, using as the chiral selector the 1-(3-aminopropyl) derivative of (+)-(5R,8S,10R)-terguride, has been developed to resolve optically active isomers by HPLC. Good resolution of structurally related racemic ergot alkaloids were obtained using water-methanol mixtures as the eluent. Analysis of the influence of the type and concentration of the organic modifier, and the pH of the buffer in the mobile phase allowed the enantioseparation of these compounds to be optimized. Determination of the optical purity of a lisuride-containig drug is reported. © 1994 Wiley-Liss, Inc.
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  • 142
    ISSN: 0899-0042
    Keywords: diastereoisomer complexes ; nuclear magnetic resonance spectroscopy ; ergot alkaloid derivatives ; haproxen enantiomers ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H NMR (600 MHz) measurements of chemical shift changes were made in acidified (DCI) CD3OD/D2O 1:9 v/v equimolar solutions of (S)- and (R,S)-6-methoxy-α-methyl-2-naphthaleneacetic acid (naproxen) in the presence of 1-(3-aminopropyl)-(5R,8S,10R)-terguride (AMP-TER). The most significant bonding interactions concurring to the formation of diastereoisomer complexes are seen as chemical shifts in proximity to the positively charged nitrogen N(6)-CH3 and of H(12), H(13), H(14) protons of the ergoline skeleton, both the adducts having an electrostatic term and different π-π stabilizing interactions. Chemical shift data exclude any contribution of the aminopropyl chain to the chiral recognition mechanism. These findings provide an experimental basis for the enantiodiscriminative process accounting for the observed chromatographic resolutions of arylcarboxylic acids on chiral stationary phases derived from AMP-TER. © 1994 Wiley-Liss, Inc.
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  • 143
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    Chirality 6 (1994), S. 564-571 
    ISSN: 0899-0042
    Keywords: achiral/chiral chromatography ; chiral HPLC ; circular dichroism ; Dictyostelium discoideum ; flavoprotein column ; fluorescence ; pteridines ; stereoconfiguration ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Optically active lumazines (biolumazine, dictyolumazine, monalumazine, and neolumazine) are prepared from the corresponding pterins by enzymatic reaction, using pterin deaminase excreted by Dictyostelium discoideum. The fluorescence properties, circular dichroism spectra, and chromatographic behavior of these lumazines are studied. D- and L-enantiomers of biolumazine, dictyolumazine, and monalumazine are separated using a chiral flavoprotein column. This column also separates the enantiomeric pterins of the threo form: monapterin and dictyopterin. However, the column does not separate the enantiomeric pterins of the erythro form: neopterin and biopterin. By coupling a reverse-phase column to the flavoprotein column, the separation of pterins and lumazines in function of their hydrophobicity, as well as the separation of the diastereomers, is achieved. This coupled achiral/chiral high-performance liquid chromatography method enables determination of the stereoconfiguration of natural lumazines by comparison with optically pure compounds. A lumazine derivative, present in the extracellular medium of Dictyostelium discoideum, is identified as D-dictyolumazine, i.e., 6-(D-threo-1,2-dihydroxypropyl)-lumazine. © 1994 Wiley-Liss, Inc.
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  • 144
    ISSN: 0899-0042
    Keywords: antiarrhythmic drug ; mexiletine ; absolute configuration ; X-ray analysis ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Data on the absolute configuration of mexiletine (MEX) do not appear to have been published, although in several published reports the configuration is referred to as (-)-(R) and (+)-(S), based on information from manufactures providing the drug stereoisomers. We demonstrate that (-)-MEX has the (R)-configuration by mean of a new stereospecific synthesis. X-Ray analysis of an optical active sample of (+)-MEX as its hydrobromide salt, obtained from chemical resolution of the racemic mixture, was carried out in order to obtain precise information on bond lengths and angles, useful for studies on structure-activity relationships. We also report the NMR analysis in presence of Eu(hfc)3 as shift reagent, which represents a simple method for the determination of enantiomeric excess (ee) in addition to the well-known chiral HPLC methods. © 1994 Wiley-Liss, Inc.
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  • 145
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    Chirality 6 (1994) 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 146
    ISSN: 0899-0042
    Keywords: cimetidine ; sulfoxidation ; urinary metabolite ; enantiomeric composition of cimetidine sulfoxide ; sequential achiral - chiral high-performance liquid chromatography ; preparative chromatographic resolution ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The individual enantiomers of cimetidine sulfoxide were resolved by preparative chromatography using a Chiralcel OC stationary phase and were characterized by the determination of optical rotation and circular dichroism spectra. Cimetidine sulfoxide was isolated from the urine of two healthy male volunteers following oral administration of cimetidine (400 mg). Urine was collected every 2 h for 12 h postdosing, after which time HPLC analysis indicated negligible recovery of the drug as the sulfoxide. Some 7% of the dose was recovered as cimetidine sulfoxide over this period. The enantiomeric composition of cimetidine sulfoxide was determined by sequential achiral - chiral chromatography using the OC phase. Over the collection period the enantiomeric ratio was found to be constant in all samples at (+/-) of 71 ± 2.5:29 ± 2.5. The enantiomeric composition of cimetidine sulfoxide was also determined in rat urine (24 h) following the administration of cimetidine (30 mg/kg po) to male Wistar rats (n = 7). The enantiomeric ratio in this case was found to be (+/-) 57 ± 2.3:43 ± 2.3. These preliminary data indicate that sulfoxidation of cimetidine is stereoselective with respect to the (+)-enantiomer and that species variation in enantiomeric composition occurs. © 1994 Wiley-Liss, Inc.
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  • 147
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    Chirality 6 (1994), S. 690-690 
    ISSN: 0899-0042
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
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    Journal of Physical Organic Chemistry 7 (1994) 
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    Keywords: Organic Chemistry ; Physical Chemistry
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    Journal of Physical Organic Chemistry 7 (1994), S. 1-8 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Semi-empirical (AM1) calculations on the 12 isomeric products and the corresponding transition states of ketene-1-azabutadiene [4 + 2] and [2 + 2] cycloaddition reactions as a model system for the reaction of ketenes with 4-iminobenzylfuran-2,3-diones are presented. A [4 + 2] type of reaction of the ketene C=C double bond leading to a six-membered lactam compound is found to be highly favoured both thermodynamically and kinetically. [2 + 2] Cycloadducts generally have significantly higher activation energies. Reactions involving the formation of a carbon-nitrogen bond proceed in most cases via attack of the nitrogen lone pair leading to a zwitterionic intermediate. Depending on the respective cycloadduct, both two-step and concerted, albeit asynchronous, processes were obtained. Based on the structures of the various transition states, some predictions with respect to substituent effects are made. Similarities to and differences from the analogous reaction of ketenimines with oxa-1,3-dienes are discussed.
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  • 150
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
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    Notes: New N-alkylation and N-arylation procedures starting from anilinomagnesium (ArNHMgBr) are reported. For N-alkylation with alkyl bromides, addition of hexamethylphosphoramide to an ArNHMgBr solution in tetrahydrofuran (THF) is effective. After heating at 55°C, N-monoalkylation product was obtained in 60-90% yield, slight dialkylation taking place. The combined use of aryliminodimagnesium [ArN(MgBr)2] with α,ω-dibromoalkanes led to N-arylazacycloalkanes. For N-arylation with iodobenzene, replacement of THF with pyridine and additional use of copper(I) iodide are effective. After heating at 115°C with iodobenzene, mono- and diarylation products were obtained, the former being predominant. The combined use of ArNHMgBr and N,N,N′,N′-tetramethylethylenediamine as the ligand of copper species is effective for elimination of diarylation and other undesired products, and leads to diarylamines in excellent yield. The method is of advantage over the conventional Ullmann and Chapman methods. The polar solvents and copper salt are effective additives for inducing ‘inert combinations’ of ArNHMgBr or ArN(MgBr)2 with alkyl and aryl halides into N—C coupling, to extend the unified view proposed for the reactivity of magnesium reagents. The difference in the roles of N—Mg and N—Cu species is discussed.
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  • 151
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Laser flash photolysis of a series of alklylbromo- and alkylfluorodiazirines in pentane at ambient temperature generates alkylhalocarbenes by decomposition of the diazirine excited states. The halocarbenes can be intercepted with pyridine to form ylides. The ylides absorb intensely between 350 and 400 nm and are fairly long lived (τ » 10 μs), making them convenient probes of the yield and dynamics of the carbene. The yield of the ylides increases with increasing pyridine concentration up to 1·5 M. At pyridine concentrations 〉 1·5 M the yield of ylide is saturated, signifying that every carbene generated in a laser pulse is captured by pyridine prior to reaction with solvent or intramolecular rearrangement. The yield of trappable carbene generated from alkylbromodiazirines closely tracks the bond dissociation energy of the C—H bond adjacent to the diazirine moiety. The data indicate that the excited states of the alkylbromodiazirines suffer C—H migration (or C—C migration with cyclobutylbromodiazirine) and nitrogen extrusion in competition with carbene formation. The yield of trappable carbene derived from the alkylfluorodiazirines is independent of the bond dissociation energy of the adjacent C—H bond. This is probably a consequence of the great thermodynamic stability of α-fluorocarbenes.
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    Journal of Physical Organic Chemistry 7 (1994), S. 28-30 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The low temperature 1H NMR spectra of 2,2-bis(3,5-dibromomesityl)ethenol in CS2-CD2Cl2 (3:7) display new signals which indicate the presence of four enol species whose OH is hydrogen bonded. Oligomerization to intermolecularly hydrogen-bonded enol dimers or tetramers is suggested.
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  • 153
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
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    Notes: Reaction of aryliminodimagnesium [ArN(MgBr)2, IDMg] with nitrobenzene (Ar1NO2) in tetrahydrofuran (THF) gives unsymmetrical (unsym) azoxybenzene, which is deoxygenated to give unsym-azobenzene. The reaction is utilized for the independent preparation of ONN and NNO isomers of unsym-azoxy compounds. The effects of the relative value of the difference between oxidation and reduction potentials of para-substituted reactants, special effects of ortho-substituents of the substrate and also effects of structure and concentration of mono- and bis-IDMg reagents were studied previously, and ‘cooperation of their aggregate excess needed for product formation’ was proposed. This unfamiliar concept for reactions of magnesium reagents was studied further. Supporting evidence was obtained from the retarding effect of trimethylene chains of nitro [3.3] metacyclophanes and the derived azoxy [3.3] metacyclophanes and also from the effect of the length of bis-IDMg's central α,ω-polymethylenedioxy chain appropriate for azoxy deoxygenation. By comparison with deoxygenation by X3P reagents (X = EtO, Me2N), the general needs of cooperation of excess magnesium reagents were confirmed and its role in their reactions is discussed.
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  • 154
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    Journal of Physical Organic Chemistry 7 (1994) 
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    Keywords: Organic Chemistry ; Physical Chemistry
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  • 155
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    Journal of Physical Organic Chemistry 7 (1994), S. 50-53 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The magnitude ρx(ρnuc) is shown to decrease with increase in the extent of bond making estimated by the kinetic isotope effect for the reactions of Y-benzoyl chlorides with anilines, XC6H4NH2, in acetonitrile at 25·0°C.
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    Journal of Physical Organic Chemistry 7 (1994), S. 31-42 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements of absorption and emission spectra, fluorescence quantum yields (Φf) and lifetimes (τf) of ω-(1-pyrenyl)alkyl para-substituted benzoates PnX (X = H, Cl, CF3, CN, NO2, with n = 1-4) were carried out in solvents of various polarity. Intramolecular interaction in the ground state is not observed in any of these compounds. PnCN (n = 2-4) shows an intramolecular exciplex emission in solvents of low to high polarity. The broad, structureless emission at longer wavelength observed in ethyl acetate solution of P1CN is ascribed to an ‘exciplex-type’ emission which does not require actual overlapping of the two chromophores. P2CF3 also shows an exciplex emission in solvents of medium to high polarity. The solvent dependence of both Φf and τf increases as the electron-withdrawing ability of the para-sustituents increases. The relationship between fluorescence quenching by electron transfer and para-substituent of PnX is discussed by means of the free energy for electron transfer, ΔGET, obtained from the oxidation and reduction potentials of pyrene and methyl para-substituted benzoates in acetonitrile, respectively. PnH, with positive ΔGET, does not show a solvent dependence of Φf, except for P1H, in which ca 40% of the fluorescence is quenched in acetonitrile. PnCl, with slightly negative ΔGET, shows more efficient quenching, but does not show exciplex emission. PnCN, PnCF3 and PnNO2 have ΔGET values between -0·36 and -0·65 eV, and their fluorescence is fairly efficiently quenched. The fluorescence of PnCN is concluded to be strongly quenched by intersystem crossing from the singlet exciplex to the locally excited pyrene, and by electron transfer from the pyrene part to the benzoate part. That the formation of a singlet exciplex is necessary for intersystem crossing in bichromophoric compounds containing pyrene is thus clearly illustrated.
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    Journal of Physical Organic Chemistry 7 (1994), S. 43-49 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Magnetic coupling between two sterically protected phenoxyl radicals through the cis- and trans-stilbene chromophores was studied by means of their EPR fine structures. While the zero-field splitting parameters D, which are governed by the magnitude of dipolar coupling, were dependent on the geometrical isomerism, the sign of exchange coupling was independent of it and dictated by the topology of the π-conjugated systems: ferromagnetic in o,m-isomers and antiferromagnetic in m,m'-isomers.
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    Journal of Physical Organic Chemistry 7 (1994), S. 68-79 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The evidence for the mechanisms proposed for aromatic nucleophilic substitution reactions by primary and secondary amines in aprotic solvents of low relative permittivity is reviewed.
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    Journal of Physical Organic Chemistry 7 (1994), S. 55-62 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The radical cation of N,N′-bis-(4-dimethylaminophenyl)pyridazine (3·+) has a near-IR band with a transition energy of 29·7 ± 0·5 kcal mol-1 (1 kcal = 4·184 kJ) in acetonitrile. This band is assigned to a Hush-type charge-transfer band, and the transition energy to the Marcus λ value for electron transfer. Such a large λ is inconsistent with previous estimates of λ for intermolecular electron transfer between mono-p-phenylenediamines and their radical cations. It agrees well with estimates of λ based on AM1 semi-empirical MO calculations, which gives the enthalpy contribution to λin at about 21 kcal mol-1 for 3·+. It is suggested that the traditional method of estimating λin by summing bond displacements weighted by force constants produces values which are significantly too low for systems such as phenylenediamines, where pyramidalization changes are important. The results suggest that λ for tetramethyl-p-phenylenediamine self-electron transfer (10/·+) has been significantly underestimated, and that this prototype organic electron transfer reaction is not as strongly diabatic as was previously concluded.
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    Journal of Physical Organic Chemistry 7 (1994), S. 63-67 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relative basicities of six monosubstituted dipolar trimethylamines (XCH2NMe2) were determined in nine different solvents from potentiometric titration. Solvation effects on basicity variations were analyzed by the solvatochromic parameters (π*, α and β). Non-specific solvation of the substituted dimethylammonium ions is not reflected adequately by the solvent's dipolarity-polarizability constant, π*. A better representation of non-specific interaction between solvents and the monosubstituted dipolar trimethylammonium ions is gained from the product of π* and the solvent dipole moment (μ). For these ions where the dipolar substituents are separated from the reaction center by one methylene unit, there is an interaction between the charge of the ammonium ion and the dipolar substituent. As a result, solvent molecules must not only solvate the dipolar substituents, but must also gain access between the lines of force of the dipolar substituent and the charge. Bulky solvents, such as nitrobenzene, cannot access adequately the region between the dipolar substituents and the reaction center to accomplish similar solvation as less bulky solvents.
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    Journal of Physical Organic Chemistry 7 (1994), S. 80-89 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measured pseudo-first-order rate constants for intramolecular formation of tetrahedral intermediates from N-2-hydroxyethylphthalimide, N-2-aminoethylphthalimide and N-2-thioethylphthalimide at pH 〉 6 are reported. The reaction is specific and general base catalysed, with β(Brønsted) values 0·44, 0·52 and 0·52 respectively. From a plot of log kb (general base rate constants) vs γ′ [the affinities of EtXH (X = O, NH, S) toward the carbonylic carbon], β′nuc values of 0·01 (with OH- as specific base), 0·25 (with imdidazole as general base) and 0·27 (with HPO42- as general base were obtained). The observed relationships pxy = ϑβ′/ - ϑpKa = -ϑ(Brønsted)/ϑγ′ = 0·03 is supported by the predictions of an energy contour diagram, which, on extrapolation to a non-stable tetrahedral intermediate, predicts a late and slightly protonated transition state for the cleavage process. At pH 〈 3, these intermediates cleave to yield only the corresponding diacylimides. These reactions are general base and acid catalysed with β 〉 0·3 and α 〈 0·1. A fast equilibrium between the intermediate and its N-protonated (amide) form is reached. The general base rupture of the latter is faster than that of the corresponding non-protonated intermediate by a factor of ca 109 - 1010-fold.
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    Journal of Physical Organic Chemistry 7 (1994), S. 96-104 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A rigorous procedure was developed for measuring the relative rates of addition of bromine atoms to eleven substituted α-methylstyrenes (1-Y, with Y = CF3, NO2, F, CN, Cl, Br, CO2Me, Me, COMe, OMe and SMe). The reaction was run in tetrahydrofuran in the presence of HBr, O2 and dibutyl peroxyoxalate at 30°C. All products were derived from the YC6H4CMeCH2Br adduct radicals, which were immediately intercepted by O2. Correlation analysis of all the data confirmed the proposition that in the absence of measurable steric effects, the relative rates for radical additions can be correlated only by a dual-parameter equation and not by a single-parameter equation. Among various combinations of σ* and σx, the (σJJ* + σmb) combination yields the best correlation.
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    Journal of Physical Organic Chemistry 7 (1994), S. 90-95 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Transfer of the cobalt-bound methyl in MeCo(III)Pc to thiophenoxide ion was studied (H2Pc is the planar macrocyclic phthalocyanine; the cobalt is held in the center in this plane). In dimethylacetamide solution, the reaction is rapid, requiring stopped flow for the kinetics, and yielding MeSPh and Co(I)Pc- in good yield. The kinetics are not simple second order, but instead approach a constant rate at high [PhS-], attributed to the reversible formation of an inert complex with PhS- occupying the vacant octahedral site in MeCo(III)Pc, on the other side of the phthalocyanine plane from the methyl group. The kinetics allow the estimation of the equilibrium constant, K, and the SN2 rate constant, k, which at 25°C have values of ca. 9·4 × 103 l mol-1 and 1·8 × 104 l mol-1, respectively. Although these values are rough, the ratio k/K is firm at 1·91 ± 0·02 s-1; this is the limit of the rate at high [PhS-]. An alternative mechanism, which is entirely consistent with the kinetics, involves a rate-determining homolysis of the Co—S bond of the same complex. The mechanism is not favored because the product yields are high for a radical combination process and alternative chain processes are kinetically unacceptable. Further, the rate constant is about what would be expected from the reactivity of other nucleophiles in SN2 reactions. Further arguments in favor of the SN2 mechanism are presented. This transfer of the methyl group from Co to S is part of the possible analogy to the vitamin B12-promoted methionine synthesis in nature. The other step in the biological, enzymatic process is the transfer of methyl from the nitrogen of N-methyltetrahydrofolate to cobalt. An attempt to model this with the very reactive N-methyl-2,6-dichloropyridinium ion was unsuccessful; the reaction took an entirely different course, presumably initiated by electron transfer, but leading to substantial loss of Cl- from the pyridine. No more than 0.5% methyl transfer took place. This system does mimic well the complete natural enzymatic process.
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    Journal of Physical Organic Chemistry 7 (1994), S. 116-116 
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    Keywords: Organic Chemistry ; Physical Chemistry
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  • 166
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    Notes: Protonation of tetrafluoro-2,11-dithia [3·3]paracyclophane and tetrafluoro-2,11-dithia [3·3]metaparacyclophane in high-acidity super acid media, namely FSO3H.SbF5 (1:1) ‘magic acid’-SO2CIF, gave their corresponding acidic disulfonium ions. Additional ring protonation to give a disulfonium-monoarenium trication was not observed. With the non-fluorinated 2,11-dithia [3·3] cyclophanes, the disulfonium ions can be ring protonated in equilibrium to give a dynamic disulfonium-monoarenium trication. Tetrafluoro [2·2]-metaparacyclophane is monoprotonated at the meta ring and gives a complex mixture of conformational isomers. Multinuclear magnetic resonance data on the cyclophane precursors and their derived cations are compared and analysed. The energies, conformations and charge distributions of the isometric fluorinated and non-fluorinated [2·2] - and dithia [3·3] cyclophanes were calculated by the AM1 and PM3 methods, respectively. In all but one case the cyclophane arenium ions predicted by theory to be energetically most favoured are those observed in solution under stable ion conditions. In agreement with experiment, the instabilities of S,S,C-cyclophane trications are also theoretically predicted.
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    Journal of Physical Organic Chemistry 7 (1994), S. I 
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    Journal of Physical Organic Chemistry 7 (1994), S. 117-121 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The kinetics of oxidation of metol (N-methyl-p-aminophenol) by thallium(III) have been studied in a perchloric acid medium. This organic compound is employed extensively in photographic work. The stoichiometry of the reaction is represented by: C6H4(OH)NHCH3 + TIIII → C6H4(O)NCH3 + TII + 2H+The kinetics indicate the rate law: \documentclass{article}\pagestyle{empty}\begin{document}$$k' = \frac{{Kk\left[{metal} \right]}}{{1 + K\left[{metal} \right]}}$$\end{document} where k′ is the pseudo-first-order rate constant. The rate constants and thermodynamic parameters for the rate-limiting step have been evaluated.
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    Journal of Physical Organic Chemistry 7 (1994), S. 122-141 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ionization constants for 214 dye molecules were calculated from molecular structures using the chemical reactivity models developed in SPARC (SPARC Performs Automated Reasoning in Chemistry). These models used fundamental chemical structure theory to predict chemical reactivities for a wide range of organic molecules from molecular structure. The energy differences between the protonated state and the unprotonated state for a molecule of interest are factored into mechanistic components including the electrostatic and resonance contributions and any additional contributions to these energy differences. The RMS deviation was found to be less than 0·62 pKa units, which is similar to the experimental error.
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    Journal of Physical Organic Chemistry 7 (1994), S. 142-146 
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    Keywords: Organic Chemistry ; Physical Chemistry
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    Notes: An empirical formula relating directly H⃛O interatomic distance to H⃛O interaction energy is used to estimate this energy in intramolecular O—H⃛O hydrogen bonds calculated for systems of known precise geometry. The values obtained were correlated with spectroscopic characteristics of the H-bond (Δv for OH bands in IR spectra and NMR chemical shifts, δ, for protons) and CNDO and INDO estimations of H-bond energy. The regressions obtained had good or very good correlation coefficients.
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    Journal of Physical Organic Chemistry 7 (1994), S. 147-152 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Cleavage reactions of α- and β-naphthylmethyl phenyl ethers and of α- and β-naphthyl benzyl ethers were studied by pulse radilysis. Transient spectra indicate that reactions occur via electron capture followed by cleavage of the resultant radical anions to give arylmethyl radicals and aryloxide ions. Product studies of extensively irradiated samples are consistent with this scheme and show patterns which are informative for radiation studies in general. The reactions were studied in several solvents. The behavior of transient spectra obtained in acetonitrile for these ethers shows clearly that radical anions of the naphthylmethyl ethers cleave more rapidly than do the radical anions of the naphthyl benzyl ethers.
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    Journal of Physical Organic Chemistry 7 (1994), S. 169-169 
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    Keywords: Organic Chemistry ; Physical Chemistry
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    Journal of Physical Organic Chemistry 7 (1994), S. 169-169 
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  • 175
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    Notes: Solvent effects on the absorption spectra of N-(p-nitrophenyl)dimethylenediamine (Ia), N-(p-nitrophenyl)trimethylenediamine (Ib), N-(p-nitrophenyl)tetramethylenediamine (Ic). N-methyl-N-(p-nitrophenyl)tetramethylenediamine (II), N-butyl-p-nitroaniline (III) and N-(o-nitrophenyl)trimethylenediamine (IV) were studied at different temperatures. Whereas II, III and IV do not show any variation in their spectra characteristics with changes in temperature, I shows a hypsochromic shift with a hypochromic effect when the temperature is increased. The Kamlet and Taft solvatochromic comparison method was applied. A strong effect of the β parameter on I and III was interpreted as being due to the hydrogen bond donor ability of the H atom in the aromatic amino groups. In I, the β influence increases with increase in temperature. These facts are explained by proposing the formation of intramolecular hydrogen bonds between amine groups in all compounds I, besides the intermolecular interactions between compounds I and the solvent. On the other hand, the values of vo, s and b for Ib are smaller than the corresponding values for Ia and Ic. Since in Ib a six-membered ring may be formed, a more stable bond is expected. Comparative 1H NMR of the aniline hydrogen for I and IV (in non-hydrogen bond acceptor solvents) shows a particular downfield chemical shift for I which suggests hydrogen bond formation. Since this effect is independent of concentration, the hydrogen bond is assumed to be intramolecular, in agreement with solvatochromic and thermochromic studies. These conclusions were corroborated by IR spectroscopy in the solid state and in chloroform solutions.
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  • 176
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reduction of 9-cyanoanthracene by two equivalents of potassium in liquid ammonia was shown to yield the 9-cyanoanthracene dianion, whereas 1-naptho- and benzonitrile gave the cyanodihydroaryl anions corresponding to the protonation of nitrile dianions at a position para to the cyano group. The 9-cyanoanthracene dianion underwent the same transformation in the presence of a stronger protonating agent, methanol. According to 13C NMR spectral data of the generated species, the cyano group extracts the negative charge from the π-electronic system: ca 0·20:0·25 e in the case of the 9-cyanoanthracene dianion and ca 0·14:0·17 e in the case of cyanodihydroaryl anions. These estimations and the general NMR pattern of π-charge distribution in all the anionic species under investigation are in accordance with data from quantum molecular orbital calculations at the PM3 and INDO levels, being reflected by the fairly good linear relationships between the changes of ring carbon chemical shifts on going to the anionic species from the respective neutral precursors on the one hand and the calculated π-charges on the other. The para-orienting effect of the cyano group in the protonation of nitrile dianions is discussed in terms of the π-charge distribution in the starting dianion and the tendency to form a most stable cyanodihydroaryl anion isomer.
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  • 177
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dipole moments, average molecular weights and IR spectra of 2-oxoidoline (I), 2-oxo-3-methylindoline (II) and 2-oxo-3,3-dimenthylindoline (III) and their N-methyl-substituted analogues were studied in CCl4 solutions at various concentrations. It was shown that the molecules with an N—B bond associate exclusively to cyclic dimers. The values of the association constants (K) were determined by IR spectrometry. Other methods gave too broad intervals of possible K values. The spectroscopic association constants of compounds I-III are very similar, 380, 350 and 370 dm3 mol-1, respectively. The vs(NH) band shift on association is 275 cm-1.
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  • 178
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    Journal of Physical Organic Chemistry 7 (1994), S. 178-180 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The volumes of activation and of reaction were measured for the reaction between sulphur dioxide and 2,3-dimethylbuta-1,3-diene to form 3,4-dimethylsulpholene. Values of ΔV and ΔV* are -33 and -35 cm3 mol-1, respectively in accordance with a concerted reaction having a very product-like transition state.
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  • 179
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    Journal of Physical Organic Chemistry 7 (1994), S. 192-195 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The secondary α-deuterium isotpe effect on the equiliburium constant (KD/KH) for the hydration of p-nitrobenzaldehyde is 1·39 ± 0·05. The Kinetic secondary α-deuterium isotope effect (KD/KH) for the addition of water to p-nitrobenzaldehyde is 1·18 ± 0·07. This result demonstrates that there is extensive carbon-oxygen bond formation in the transition state for addition of water to the carbonyl group of p-nitrobezaldehyde.
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  • 180
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    Journal of Physical Organic Chemistry 7 (1994), S. 181-191 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: [2.1.1] Cryptated lithium salts of a wide range of CH-acids were studied spectrophotometrically and conductimetrically in solvents of low polarity. Such salts exist in media of different dielectric constants in the form of cryptand-separated ion pairs which are identical in their spectral and conductance properties with common solvent-separated ion pairs. No formation of higher ionic clusters was observed for the studied ions at concentrations below 10-3 mol-1 even in the benzene. The relative equilibrium acidities in benzene, N-methylmorpholine and tetrahydrofuran for a number of CH-acids are reported. Solvent polarity does not influence the cryptate ion-pair acidity of the investigated compounds. The relative free ion acidities were calculated for some of the studied acids in different solvents by combination of the ion-pair acidity values with the conductimetric data on dissociation constants of the cryptate ion pairs. A linear relationship between the free ion acidity and the reciprocal of the dielectric constant was found. An extrapolation method is suggested for the calculation of gas-phase acidity from the data obtained in solution.
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  • 181
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    Journal of Physical Organic Chemistry 7 (1994), S. 196-206 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Structural effects on the melting points of substituted alkanes, both branched and unbranched, ranging in length from 1 to 19 carbon atoms, were successfully correlated with a variant of the intermolecular force equation which included a variable capable of accounting for the packing energy contribution of the alkyl group. The final data set had 366 data points. The regression equation obtained accounted for 91·85% of the variance of the data with a standard error of 17·9 K. Twenty-nine data points could not be included in the correlation; nine of these are carboxamides. The contributions of the polar variables are slightly larger than those of the nonpolar variables while the contribution of structural variation in the substituent is greater than that in the alkyl group. It will be necessary to determine appropriate values of the packing parameter if compounds with chains longer than 20 carbon atoms are to be included in the model.
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  • 182
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    Journal of Physical Organic Chemistry 7 (1994), S. 207-217 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A semi-empirical configuration interaction (CI) algorithm is presented for predicting the ground-state spin multiplicity of open-shell systems. The computed energy gaps ΔE(LS—HS) of model systems, Y-phenyl-X-phenyl-Y, where Y is a nitrene or nitroxide radical and X is an exchange coupling unit, are critically compared with the available experimental data. The current method has attenuated the deficiencies of the earlier algorithm proposed by Lahti and Ichimura and the predictions are qualitatively clearer, facilitating the classification of high- and low-spin topologies for isomeric species. The relative effectiveness of different exchange couplers can be discerned semi-quantitatively, and several new exchange couplers are described. The reasons for the qualitative failure of the earlier algorithm are discussed.
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  • 183
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    Journal of Physical Organic Chemistry 7 (1994) 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
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  • 184
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    Journal of Physical Organic Chemistry 7 (1994), S. 218-220 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In the hydride transfer of Leuco Crystal Violet to form the Crystal Violet, cation, the role of cyanomethylene acceptors was found to be essentially different from that of p-benzoquinones, both previously believed to act as π-acceptors in the same manner.
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  • 185
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: In constrast with recent molecular orbital calculations on the decarboxylation of O-protonated 2-oxetanone, this experimental work indicates that no decarboxylation of this cation occurs in sulphuric acid solution up to 150°C, but instead a clean isomerization to protonated acrylic acid takes place. Parallel theoretical work shows that the gas-phase model is too crude to account successfully for the experimental facts obtained in acidic media. However, the latter are well reproduced when the effect of the solvent is taken into account. The present findings do not necessarily invalidate the reaction mechanism currently accepted to explain the rate enhancement and change of stereochemistry accompanying the decarboxylation of 3,4-disubstituted 2-oxetanones under acid catalysis.
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  • 186
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The enol-keto tautomerism of the Schiff bases formed by pyridoxal 5'-phosphate (PLP) with ethylenediamine (Etd) and ethylamine (Et) was studied by electrochemical and spectrophotometric methods. The spectroscopic results revealed differences between the two reactions, i.e. the enolimine/ketoenamine ratio observed in PLP-Etd mixture is higher than that of PLP-Et. The differences observed in the electroreduction mechanism and stability of the Schiff bases formed provide additional evidence for an unusually high concentration of enolimine in PLP-Etd in buffered aqueous solutions.The results are consistent with a cyclic structure such as that previously proposed by Robitaille et al. [J. Am. Chem. Soc. 111, 3034-3047 (1989)] on the basis of spectroscopic data. Protonation of the terminal amino group of the Etd moiety in the Schiff base involves the formation of the cyclic species. The low basicity of ethylenediamine favours the formation of similar concentrations of the enol and keto tautomers of the Schiff base at neutral pH. This behaviour, also observed in the Schiff base formed by PLP and polylysine, may be involved in coenzyme-protein linkages.
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  • 187
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 2,2-Dimethyl-1-(p-methoxyphenyl)propyl p-nitrobenzoate (ROPNB) was subjected to solvolysis in phenol in the presence of tetrabutylammonium [carboxy-13C]-p-nitrobenzoate, in which the ‘common ion rate depression’ was confirmed to arise at the stage of the second ion-pair intermediate (Int-2). The unchanged substrate recovered at 46% reaction contained the isotopically labelled leaving group, indicating the occurrence of common ion exchange to the extent of 41-46%. In the solvolysis of the optically active substrate under identical conditions, the unchanged substrate was recovered with 51·4% racemization and ROPh was produced with slightly (1·56%) retained configuration, similarly to the solvolysis in the absence of the common ion salt. These isotope-tracer and stereochemical outcomes indicate that the common ion exchange in this solvolysis system should be attributable to the retentive nucleophilic attack on Int-2 by the common ion salt via a quadrupole (four-centre ion pair) transition state, accompanying the common ion rate depression, and they suggest that the special salt effect also should proceed by an analogous anion-exchange mechanism to that for the common ion effects.
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  • 188
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    Journal of Physical Organic Chemistry 7 (1994), S. 256-258 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The relative thermodynamic stabilities of 2-propenylbenzene (allylbenzene), and the E and Z forms of 1-propenylbenzene were determined over the temperature range 50-170°C by chemical equilibration in DMSO solution with t-BuOK as catalyst. The values of the thermodynamic parameters ΔG⊖, ΔH⊖ and ΔS⊖ at 298·15 K for each isomerization reaction between the title compounds were evaluated.
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  • 189
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    Journal of Physical Organic Chemistry 7 (1994), S. 251-255 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: According to quantum chemical calculations, the anion radical of disilene adopts a syn- or anti-pyramidal geometry. The former is not a stable entity on the electronic hypersurface and it decreases further in energy by rotation of the Si-Si bond. Energy optimization of various structural alternatives reveals for the anion radical an Si-Si bond slightly longer than a single bond. The anti geometry prefers a C2h geometry whereas the syn geometry resembles a silylene coupled with a silylene radical anion. The fragmentation of disilene into two silylene units is less exothermic for the neutral species than for the anion (radical), as examined by the ab initio calculations.
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  • 190
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    Journal of Physical Organic Chemistry 7 (1994), S. 259-267 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The conformational properties of diethyl disulphide, a model compound for the disulphide bridges in peptides and proteins, were studied with ab initio methods. Stationary point structures were optimized at the HF/6-31G* level with consideration of electron correlation in subsequent single-point MP2 calculations. The six energy minima were also optimized at the MP2/6-31G* level with calculation of zero-point vibrational frequencies and thermal corrections. Additional single-point MP2 energy calculations employed larger basis sets up to 6-311G(2d, p). With positive disulphide chirality, the global energy minimum is a ‘spiral’ conformation with gauche + C-C-S-S torsion angles. The further stability order for energy minima deviates from previous ab initio results. In particular, the extended trans,trans conformer is subject to a significant relative destabilization on inclusion of electron correlation in the calculations and is only the fifth most stable energy minimum with estimated ab initio ΔH298 = 5·13 kJ mol-1. The results presented are relevant for the discussion of conformational properties for the structurally equivalent disulphide bridges in polypeptides and calculations of relative energies with molecular mechanics methods.
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  • 191
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    Journal of Physical Organic Chemistry 7 (1994) 
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    Keywords: Organic Chemistry ; Physical Chemistry
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  • 192
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Calculations were carried out to study the validity of σ-scales for hydrogen abstraction from substituted toluenes by tert-butyl, tert-butoxyl and tert-butylperoxyl radicals. Rate constants were compiled and evaluated from the literature for meta- and/or para-substituted toluenes. The substituents were characterized by factored ionic sigmas (σI, σR, σR+), ionic scales (σ, σ+) and various radical sigmas (σσ). The dependence of log k values on these substituent descriptors was investigated using ‘stepwise linear regression’ and ‘all possible regression’ methods. The following predictive equations can be recommended: for tert-butyl radicals, at 321 K: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {\log \,k_1 \, = \,1.024\, + \,0.776\,\sigma _1 \, + \,0.653\,\sigma _{\mathop C\limits^. }} \quad {(R\, = \,0.8137)} \end{array}$$\end{document} for tert-butoxyl radicals, at 313 K: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {\log k_2 = 5.529 - 0.623\sigma ^ +} \quad {(R = 0.9376)} \end{array}$$\end{document} and for tert-butylperoxyl radicals, at 303 K: \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{*{20}c} {\log k_3 = - 1.410 - 0.810\sigma + 0.337\sigma _{\mathop C\limits^. } } \quad {(R = 0.9628)}\end{array}$$\end{document} The results suggest that there is no unversal radical scale for hydrogen abstraction reactions, that the rate is primarily influenced by polar factors (inductive, resonance) and that only two radical scales (σĊ and σα·) are appropriate, showing a small, yet significant, role of radical stabilization.
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  • 193
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    Journal of Physical Organic Chemistry 7 (1994), S. 268-271 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Acidities of a representative range of carbon acids were calculated by various levels of ab initio theory and by the semi-empirical methods AM1 and PM3 in order to ascertain what level is necessary in order to obtain consistently reliable results. The semi-empirical methods give good agreement with experiment in about a third of the cases, but are significantly, and sometimes seriously, in error for the rest. The 3-21G ab initio method consistently underestimates acidities by a substantial amount. The best results were obtained at the MP2/6-31 + G*//6-31 + G* level. Higher level Møller-Plesset corrections worsened the agreement with experiment.
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  • 194
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    Journal of Physical Organic Chemistry 7 (1994), S. 273-279 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nucleophilic substitution reactions of benzoic anhydrides, in which one of the rings is substituted, with anilines were investigated in methanol. The product-formation step coincides with the rate-limiting step so that the two rate constants, kXZ and kXZ, for the competitive reaction pathways can be dissected. The two cross-interaction constants, ρXY and ρXY, especially an unusually large magnitude of the latter, indicate that the reaction proceeds by a frontside SN2 attack on either one of the caronyl carbon with a strong interaction between the nucleophile (X) and the leaving group (Z). The mechanism is also supposed by the trends in the activation parameters.
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  • 195
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    Journal of Physical Organic Chemistry 7 (1994), S. 280-286 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The 15N chemical shifts of various m- and p-substituted anilides and related derivatives, ZNHC6H4Y [Z = C6H5CO, CH3CO, CF3CO, CH3SO2, (C6H5O)2PO and H], were correlated with σ- constants. With all series of anilides investigated, the plotted points for the m- and p-substituted derivatives tend to be separated from each other and to lie on two different regression lines. Reinvestigation from this point of view revealed that similar separations occur generally with substituted aniline derivatives. The anomalous polar substituent effect was ascribed to the very large contribution of a resonance effect. In addition, the local π-polarization effect causes a negative slope for the m-substituted series in the case of carboxylic anilides.
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  • 196
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    Journal of Physical Organic Chemistry 7 (1994), S. 287-295 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The spontaneous hydrolysis of p-nitrobenzyl cellulose xanthate (CelXNB) with a degree of substitution (DS) in the range 2-9 was studied in 10% aqueous ethanol at pH 10, and was followed spectrophotometrically by the appearance of p-nitro-α-toluenethiol, in a continuous-flow system where the reactor was shaken. CelXNB was characterized by solid-state 13C NMR spectra. The reaction occurs through two parallel processes due to two xanthate ester groups with different reactivities. The fast hydrolysis was ascribed to the reaction of the C-2 + C-3 isomers, whereas the slow hydrolysis was due to the C-6 isomer. The percentage of the latter is much higher than C-2 + C-3. The solvent isotope effect of the fast hydrolysis (k′H2O/)k′H2D 11 was 2·22 ± 0·16 and the proton inventory indicated that there is only one proton transfer involved in the transition state, where a second water (or a neighbouring OH group) acts as a general base. The entropy of activation of the fast hydrolysis was only 3·3 ± 0·8 e.u., suggesting that the water molecules involved are highly oriented with respect to the coordinates required to reach the transition state. It is proposed that they form part of the three-dimensional hydrogen-bonded ice-like structure that involves the cellulose matrix.
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  • 197
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    Journal of Physical Organic Chemistry 7 (1994), S. 296-302 
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    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The aromatic odd-alternant phenalenyl anion and a number of its derivatives were prepared in order to study the perturbation of this conjugated anion by methyl and methoxy groups. The conjugated anions were studied by means of 1H and 13C NMR spectrometry, alkylation experiments and semi-empirical calculations. It was found that a substituent at a charged carbon atom perturbs the entire conjugated system, whereas substituents at inactive (uncharged) carbon atoms have a large effect on the positions ortho to the substituent.
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  • 198
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    Keywords: Organic Chemistry ; Physical Chemistry
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    Topics: Chemistry and Pharmacology , Physics
    Notes: Cubane diester crown ethers were tested as ion-selective electrodes in poly(vinyl chloride) (PVC) membranes. The four ionophores studied proved to be good K+ neutral carriers, showing Nernstian and near-Nernstian responses to this ion, in the range 10-4-10-1 M. The fixed interferences method was used to determine relative selectivity coefficients for all the electrodes. The highest selectivity for potassium relative to sodium, lithium, calcium and magnesium ions using potassium tetrakis(p-chlorophenyl)borate (KTpClPB) as a resistance modifier and NPOE as a plasticizer was obtained with the 1,4-cubyl diester-25-crown-7 ether ionophore. The effects of KTpCIPB on membrane selectivity were assessed; its removal was found to increase the selectivity of the four ionophores for potassium relative to cesium, sodium, calcium and magnesium ions with minimal effects on lithium and ammonium ions. The compounds tested exhibited a fast Nernstian response to changes in K+ concentration which was stable to within 〈100 μV h-1.
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  • 199
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    Journal of Physical Organic Chemistry 7 (1994), S. 323-323 
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    Keywords: Organic Chemistry ; Physical Chemistry
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  • 200
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    Journal of Physical Organic Chemistry 7 (1994), S. 309-315 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The hydride transfer reactions of 4,4′-bis(dimethylaminophenyl)methane (Michler's hydride) with p-benzoquinones were studied. The rate of formation of Michler's Hydrol Blue was followed spectrophotometrically. The second-order rate constants and the activation parameters were estimated. The formation of a charge-transfer complex was observed at low temperatures. Stable and unstable paramagnetic species formed during the reactions were assigned by ESR spectroscopy. The observed kinetic behaviour and the stoichiometry were in line with those previously obtained for the systems involving Leuco Crystal Violet, Leuco Malachite Green and Leuco Bindschedler's Green. Hence the reaction is considered to proceed according to the so-far accepted multi-step mechanism. However, when tetracyano-p-quinodimethane or tetracyanoethylene was used as a π-acceptor, a comparatively stable radical ion pair was formed as a result of a one-electron transfer, followed by the gradual formation of Michler's Hydrol Blue. The kinetic behaviour and the stoichiometry of the reaction were examined, together with the enhanced kinetic effects of added triethylamine. A modified mechanism for these systems is proposed. The role of cyanomethylenes was found to be essentially different from that of p-benzoquinones, and therefore π-acceptors are divided into two groups of cyanomethylenes and p-benzoquinones.
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