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  • 1
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 26 (1988), S. 191-196 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Perimidines ; Perimidinium salts ; 1H NMR ; Tautomerism ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of some 1- and 2-substituted perimidines and perimidinium salts are discussed and assigned. Although the spectra of most of the 2-substituted perimidines are comparatively simple, several examples display 13C and 1H spectral characteristics indicative of inhibition of prototropic tautomerism.
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  • 2
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    Organic Magnetic Resonance 26 (1988), S. 281-286 
    ISSN: 0749-1581
    Keywords: Ribonucleosides ; Solid-state ; 13C NMR ; Residual 13C ; 14N dipolar coupling ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C CP/MAS NMR spectra of nitrogen-containing compounds often show complex signals when recorded at low field strengths. This effect is due to the 13C, 14N residual dipolar coupling which is not averaged to zero by magic-angle spinning. Solid-state 13C NMR spectra at 25 MHz of ribonucleosides are analysed on the basis of the isotropic chemical shifts measured at 50 MHz, together with the asymmetric splittings caused by the presence of 14N calculated using a first-order equation. X-ray diffraction and NQR data, together with several assumptions regarding the quadrupole tensor at each 14N site, are used to obtain a successful spectral simulation.
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  • 3
    ISSN: 0749-1581
    Keywords: Asparagus officinalis ; Liliaceae ; Spirostanol glycoside ; 13C NMR ; DEPT ; 2D heteronuclear chemical shift correlation ; COSY ; Relayed coherence transfer ; NOESY ; INEPT ; Indirect detection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complete 13C and 1H assignments for the oligosaccharide segment of a novel spirostanol glycoside were derived, and structural proof obtained, using a combination of DEPT, heteronuclear chemical shift correlation, homonuclear relayed coherence transfer, absolute value COSY, phase-sensitive double quantum filtered COSY, NOESY, INEPT and proton-detected long-range heteronuclear shift correlation via multiple quantum coherence.
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  • 4
    Electronic Resource
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    Organic Magnetic Resonance 26 (1988), S. 992-1002 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Prediction of 13C spectra ; Molecular modelling ; Molecular mechanics application ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A methodology is described which allows the rationalization of the 13C chemical shifts of a variety of compounds including alkanes, alcohols and ketones. The geometries of 250 rigid compounds were computed by the MM2 force field. Multiple linear regression analysis was used to model the 13C shifts from topological, geometric and energetic parameters. Among these parameters, the most important were those corresponding to interatomic distances, hybridization state of the quaternary carbons and energetic parameters. The final result is a rationalization of the 13C chemical shifts with an average RMS error of 1.25 ppm.
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  • 5
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    Organic Magnetic Resonance 26 (1988), S. 1037-1038 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Pyrroles ; Bromopyrroles ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR chemical shift assignments of unbrominated, monobrominated and dibrominated pyrrole 2-trichloroketones, esters and amides are presented.
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  • 6
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    Organic Magnetic Resonance 26 (1988), S. 1041-1046 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; Ranitidine ; Spin-lattice relaxation rates ; Conformation in solution ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Conformational and dynamic features of ranitidine were delineated by 1H and 13C NMR 1D and 2D spectroscopy. Spin-lattice relaxation rates and homo- and hetero-nuclear NOEs were measured. An extended conformation was shown to predominate in solution, with restricted segmental motion. The main reorientational motion and some of the internal motions were characterized in terms of stochastic internal motion around a molecular axis that reorients isotropically. Selective irradiation methods were used to obtain relevant conformational parameters.
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  • 7
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    Organic Magnetic Resonance 26 (1988), S. 1103-1108 
    ISSN: 0749-1581
    Keywords: Sulphones ; 13C NMR ; Geminal 13C,13C coupling ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A measurable coupling between carbon atoms through the SO2 group is observed in a series of structurally diverse sulphones. In open-chain (single coupling path) sulphones this 2J coupling ranges from 5.5 to 27.2 Hz, while in cyclic (multiple coupling path) sulphones values ranging from 4.3 to 21.6 Hz are observed. Sulphides and sulphoxides do not exhibit a corresponding coupling of comparable magnitude. A positive sign for this coupling is derived from the data of cyclic sulphones. Whereas substituents and branching at the coupling termini exert minor influences on the coupling, the most important factor determining the magnitude of the 2J(CSC) coupling is the hybridization of the coupling carbon atoms. A linear relationship between the 2J value and the s character product of the C—S bond forming C orbitals is estalished.
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  • 8
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    Organic Magnetic Resonance 26 (1988), S. 124-128 
    ISSN: 0749-1581
    Keywords: Reaction of pyrrole with formaldehyde ; Hydroxymethylpyrroles ; 13C NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complex course of the reaction of pyrrole with formaldehyde has been completely elucidated by quantitative 13C NMR spectroscopy using the inverse-gated decoupling technique. The final product is 2,5-bis(hydroxymethyl)pyrrole (with a free 1-position), but three main intermediates containing 1-hydroxymethyl groups were identified, and the rise and subsequent fall of their populations followed. The intermediacy of additional compounds (formals) also renders the reaction more complex. The molar fractions of four hydroxy-methylpyrroles present in the reaction mixtures were calculated from the 13C NMR data and plotted against time. At 45 and 65°C pyrrole reacted completely with formaldehyde in 1 h and in less than 30 min, respectively. This work illustrates the utility of the 13C NMR investigation of an industrially important reaction.
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  • 9
    ISSN: 0749-1581
    Keywords: High-resolution solid-state ; 13C NMR ; Chemical shift non-equivalence ; Methoxybenzenes ; Phenols ; meso-Hexestrols ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR spectra of para-substituted methoxybenzenes and phenols were recorded in the solid state to gain an insight into the manner and origin of substantial peak splittings in the ortho (up to 9.2 ppm) and meta (up to 2.5 ppm) carbon signals. It was difficult to account for these peak splittings only by the steric interaction with the methyl group of the substituent, because their magnitude varied widely from 4.6 to 9.2 ppm with a variety of substituents at the para position, and the meta carbon peaks are also split into doublets. Instead, it was found that the electron density non-equivalence between the two ortho and the two meta carbons is mainly responsible for the splittings, as manifested by the presence of an approximate linear relationship between the displcements of the 13C NMR peaks and total electron density. The observed additional splitting in the 13C NMR spectra of meso-hexestrol and its methyl or ethyl ether(s) in the solid state was similarly explained. Stereochemical features of these molecules in the solid state are discussed on the basis of the 13C NMR data.
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  • 10
    Electronic Resource
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    Organic Magnetic Resonance 26 (1988), S. 433-435 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 2D NMR ; Liquid crystals ; 4-(trans-4-Alkylcyclohexyl)benzonitriles ; 4-(trans-4-Alkenylcyclohexyl)benzonitriles ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complete 13C and 1H spectral assignments for two series of liquid crystals in CDCl3 solution were made. The 4-(trans-4-alkylcyclohexyl)benzonitriles had propyl-to pentyl-substituted alkyl chains, whereas the 4-(trans-4-alkenylcyclohexyl)benzonitriles had varying positions of the alkenyl bond. 13C and 1H chemical shifts and 13C—1H scalar coupling constants are reported.
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  • 11
    ISSN: 0749-1581
    Keywords: 13C NMR ; 31P NMR ; 6-Aryloxydibenzo [d, f] ; [1,3,2] dioxaphosphepin ; 6-oxides/sulphides ; 3-Cyclohexyl-6-(1, 1-dimethylethyl)-3, 4-dihydro-2-aryloxy-2H-1,3,2-benzoxazaphosphorine 2-oxides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C And 31P NMR chemical shifts and 13C—31P coupling constants of 26 6-aryloxydibenzo [d, f][1,3,2] dioxaphosphepin 6-oxides/sulphides and 3-cyclohexyl-6-(1, 1-dimethylethyl)-3, 4-dihydro-2-aryloxy-2H-1,3,2-benzoxazaphosphorine 2-oxides are reported. The assignments are supported by SFORD spectra.
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  • 12
    ISSN: 0749-1581
    Keywords: 13C NMR ; 13C, 1H and 13C, 19F spin-spin coupling constants ; (η6-Arene)tricarbonylchromium complexes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Spin-spin coupling between carbonyl carbons and aromatic protons (or fluorine atoms) in several (η6-arene)tricarbonylchromium complexes has been observed for the first time. The values of the coupling constants are of the order of 0.6 Hz for protons and 2 Hz for fluroine, and seem to depend on the electron-donating properties of the aromatic substituent.
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  • 13
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    Organic Magnetic Resonance 26 (1988), S. 1109-1112 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Dimeric β-carbolines ; Azacarbazoles ; 9H-Pyrido[3,4-b]indoles ; Carbazole ; derivatives ; Stereochemical effects ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR spectra of a series of derivatives of carbazole and azacarbazole (norharmane or 9H-Pyrido [3,4-b]indole) are reported. The dependence of 1H and 13C shieldings on molecular geometry is discussed briefly.
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  • 14
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    Organic Magnetic Resonance 26 (1988), S. 37-41 
    ISSN: 0749-1581
    Keywords: 13C NMR ; optically active cyclohexanamines ; diestereomeric 2-methyl-N-(1-phenylethyl) cyclohexamines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of optically active primary and secondary 2-substituted cyclohexanamines were measured and the chemical shifts were unequivocally assigned. Similar studies were made with four diastereomeric 2-methyl-N-(1-phenylethyl)cyclohexanamines with three chirality centres.
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  • 15
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    Organic Magnetic Resonance 26 (1988), S. 85-88 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; 12-Substituted-14β-hydroxy steroids ; 14α-Steroids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: γgauche effects of 12-substituted-14β-hydroxy- and 14α-steroids were studied by 1H and 13C NMR spectroscopy. A linear correlation was found between the 1H chemical shift of 4H-17 and the 13C shift of C-17 for C-12-substituted steroids. This correlation can be explained by steric interactions.
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  • 16
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    Organic Magnetic Resonance 26 (1988), S. 475-481 
    ISSN: 0749-1581
    Keywords: Trichothecene mycotoxins ; Apotrichothecene ; 10,13-Cyclotrichothecane ; 13C NMR ; 2D NMR ; 1H—13C ; NOE difference spectra ; Spin-echo J modulation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A general strategy, using well established techniques, is outlined for the assignment of signals in the 13C NMR spectra of the trichothecene mycotoxins and some related rearrangement products. Heteronuclear NOE difference spectra were employed to assign resonances from quaternary carbons. An example of the use of spin-echo J modulation is given.
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  • 17
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    Organic Magnetic Resonance 26 (1988), S. 117-119 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; 2D NMR ; Diterpenoids of Coleus forskohlii ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereochemical assignments of coleonol-B (1), coleonol-D (2) and coleosol (3) were accomplished by 2D 1H—1H (COSY), 1H—13C (hetero COSY), NOE difference NMR spectroscopic, stereospecific coupling constant and selective heteronuclear spin decoupling studies. The complete 13C chemical shift assignments of 2, 3 and coleol (4) were made for the first time. The earlier 1H chemical shift assignments were corrected and the stereostructure of coleonol-D was reassigned.
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  • 18
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    Organic Magnetic Resonance 26 (1988), S. 129-133 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Substituent parameters ; Hydroxymethyl group ; Pyrrole ; Furan ; Imidazole ; 5,5-Dimethylhydantoin ; Thiophene ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C spectra of the hydroxymethyl derivatives of pyrrole, furan, 5,5-dimethylhydantoin, imidazole, thiophene, pyrazole, and phenol have been studied and assigned. The substituent parameters for the hydroxymethyl group in pyrrole, thiophene, furan, and imidazole were determined.
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  • 19
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    Organic Magnetic Resonance 26 (1988), S. 185-190 
    ISSN: 0749-1581
    Keywords: Matrine ; 13C NMR ; 1H NMR ; 2D NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The stereochemical and structural analysis of matrine was carried out using nuclear magnetic resonance spectroscopy. Several methods, including 13C—1H two-dimensional shift correlation spectroscopy, 1H—1H two-dimensional correlated spectroscopy and measurements of vicinal 1H—1H coupling constants were used for chemical shift assignments and configurational analysis. Nuclear Overhauser effect difference spectroscopy was used to establish the sterochemistry. This investigation demonstrates the power of two-dimensional NMR techniques and the nuclear Overhauser effect (NOE) in the structural determination of natural products.
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  • 20
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    Organic Magnetic Resonance 26 (1988), S. 228-235 
    ISSN: 0749-1581
    Keywords: Cadinanes ; Bicadinane ; 2D 1H NMR ; 13C NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two-dimensional 1H and 13C shift-correlated NMR experiments have been used for the unambiguous assignments of all proton and carbon chemical shifts of two cadinanes and bicadinane.
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  • 21
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    Organic Magnetic Resonance 26 (1988), S. 303-306 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Substituent chemical shifts ; Hydrogen bonding ; Substituted pyridine N-oxides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aromatic 13C chemical shifts of 4- and 3-substituted pyridine N-oxides in aprotic and protic solvents are reported and discussed. Changes in chemical shifts caused by hydrogen bonding and protonation are much smaller than those induced by a substituent, and are not related to the pKa values of N-oxides. Since the effect of hydrogen bonding is not in the same direction as that due to the substituent effect, the estimation of proton transfer from measured chemical shifts is not possible in complexes of pyridine N-oxides with trifluoroacetic acid. A linear correlation is obtained between the ipso carbon substituent chemical shifts of 4- and 3-substituted pyridine N-oxides and mono-substituted benzenes, which supports the suggestion that electronic factors other than Δq are more important for the ipso carbon.
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  • 22
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    Organic Magnetic Resonance 26 (1988), S. 327-333 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Deuterium isotope effects ; Conformational equilibrium ; Temperature dependence ; Cyclic and acyclic ketones ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclic ketones from cyclobutanone to cyclohexadecanone were labelled with deuterium in the α-position. The deuterium isotope effect on the 13C NMR spectra was measured and in some cases was indicative of perturbation of conformational equilibrium. Similar effects were observed with acyclic ketones. The results were confirmed by temperature-dependent measurements and molecular mechanics calculations.
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  • 23
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    Organic Magnetic Resonance 26 (1988), S. 445-448 
    ISSN: 0749-1581
    Keywords: Phenol-triethylamine complexes ; Ion pair-molecular complex tautomerism ; 13C NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The tautomeric equilibria in phenol-triethylamine complexes have been quantitatively investigated. A method of calculation of thermodynamic parameters based on reproducing the temperature dependences of 13C chemical shifts is described. The results are in agreement with UV and IR predictions for similar complexes. The chemical shifts characterizing molecular forms of the complexes depend on the type of phenol derivative.
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  • 24
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    Organic Magnetic Resonance 26 (1988), S. 665-670 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Carbonyl compounds ; Thiocarbonyl compounds ; Linear relationships ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C spectra of nine novel and fifteen known derivatives YC(:X)Z with X = O or S are reported and compared with literature data. Two linear relationships between 13C=O and 13C=S are established depending on whether or not Y or Z is linked through an O atom to the C=X group. General equations for 13C=O and 13C=S in terms of the attached groups are also deduced. The 13C chemical shifts of n-butyl and n-octyl groups attached to the heteroatoms in this series of compounds are recorded and discussed.
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  • 25
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    Organic Magnetic Resonance 26 (1988), S. 721-722 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1-(N-Piperidino) cyclohexanenitriles ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of nine 1-(N-piperidino) cyclohexanenitriles and of 1-dimethylaminocyclohexanenitrile have been recorded and assigned.
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  • 26
    ISSN: 0749-1581
    Keywords: 13C NMR ; 2D NMR ; Bleomycin A2 ; Bleomycin A2-zinc complex ; Complete assignment ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR spectra of free bleomycin A2 at pH 4 and 6.7 and of its zinc complex at pH 6.7 were completely assigned by making use of two-dimensional 1H—13C correlated spectroscopy. Differences in resonance positions between the spectra of the free bleomycin at pH 4 and 6.7 are observed for the β-hydroxyhistidine and the β-aminoalanine residues, obviously because of protonation/deprotonation of these moieties in the pH region considered. Also, shifts are observed for the carbon resonances of the gulose residue. Upon complex formation between zinc(II) and bleomycin large 13C shifts are observed for the carbon atoms in the pyrimidinepropionamide, β-hydroxyhistidine, β-aminoalanine, α-L-gulose and α-D-mannose fragments. Although for some residues the observed shifts correspond with the position of the zinc(II) binding sites in bleomycin proposed on the basis of earlier 1H NMR experiments, a simple correlation between the location of the zinc(II) binding sites and the 13C shifts cannot be drawn.
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  • 27
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    Organic Magnetic Resonance 26 (1988), S. 813-816 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; Bis(1,1-dimethylethyl) disulfide ; Bis(1,1-dimethylethyl) trisulfide ; sulfinothioic acid S-esters ; sulfonothioic acid S-esters ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR and 1H NMR spectra of bis(1,1-dimethylethyl) disulfide and bis(1,1-dimethylethyl) trisulfide and their oxygenated derivatives, including sulfinothioic acid S-esters and sulfonothioic acid S-esters, have been studied. Deshielding βSO and βSO2 effects and shielding γSO and γSO2 effects are observed. The NMR spectra of tert-butyl polysulfides and the influences of sulfur atoms are also compared and discussed.
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  • 28
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    Organic Magnetic Resonance 26 (1988), S. 33-36 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Diamantanoid compounds ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of eleven hydroxy and oxo derivatives of methyl esters of 1- and 4-diamantane carboxylic acids, three hydroxy derivatives of diamantanone and six dibromo derivatives of diamantane have been measured in CDCl3 or C6D6 solutions. The signals were assiged by the additivity rule. The 13C NMR spectra of all compounds were described by two parameters, e.g. the sum of the 13C chemical shifts of all carbon atoms in the measured compounds (SCCS) and the ratio of the number of carbon atoms (Nc) and theoretical number of signals (Ns).
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  • 29
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    Organic Magnetic Resonance 26 (1988), S. 8-13 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 15N NMR ; 1,2-Benzisoxazole 2-oxides ; 1,2-Benzisoxazoles ; 2-Hydroxyaryl ketoximes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C and 15N chemical shift assignments of a number of 1,2-benzisoxazole 2-oxides and their deoxygenated analogues are reported and discussed. Similarly, assignments for some of the precursors to the N-oxides, o-hydroxyaryl ketoximes, are reported. In the N-oxides the “push-pull” effect of the N—O dipole is largely localized on the isoxazole unit. A large (ca 39 ppm) upfield shift of the C-3 resonance is caused by the exocyclic oxygen whereas C-7a and, to a lesser extent, C-6 are the most heavily deshielded nuclei. The substituents do not have a significant effect on the C-3 resonance, whereas their effect on the carbocyclic carbons is more pronounced, the most markedly affected being the C-4 and C-6 nuclei. N-Oxidation of 1,2-benzisoxazole causes a large (50.5 ppm) shielding of the 15N nucleus.
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  • 30
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    Organic Magnetic Resonance 26 (1988), S. 211-213 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 19F NMR ; 4-Substituted bicyclo[2.2.2]octane-1-carbonyl fluorides ; SCS ; Polar field parameters ; Polar field susceptibility parameters ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fluorine-19 substituent chemical shifts (SCS) are reported for a series of 4-substituted bicyclo[2.2.2]octane-1-carbonyl fluorides containing a limited but a representative number of dipolar substituents. The 19F SCS, which cover a very narrow range (〈0.5 ppm), are found to correlate poorly against polar field parameters (σF). Polar field susceptibility parameters (ρF) for the fluorine probe were determined indirectly and their origin is briefly discussed in the light of the carbonyl 13C SCS which reflect π polarization of the COF group.
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  • 31
    ISSN: 0749-1581
    Keywords: 13C NMR ; Catechin derivatives ; Cyanidan-3-ol derivatives ; (2R-trans)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol derivatives ; Bromocatechin derivatives ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of 21 catechin derivatives substituted at C-6/C-8 by bromine and/or hydrogen and at oxygen by methyl, acetyl and/or hydrogen have been analysed in deuteriated acetone and chloroform. When a methoxy group is flanked by two bulky ortho substituents (6-Br and C-4), the MeO and ortho/para ring carbons (C-4a, C-6, C-8) are deshielded owing to steric inhibition of resonance, which permits a distinction between 6- and 8-substituted catechin methyl ethers. Hindered acetoxy groups do not give rise to this phenomenon.
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  • 32
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    Organic Magnetic Resonance 26 (1988), S. 552-558 
    ISSN: 0749-1581
    Keywords: Methylindoles ; 13C NMR ; Isotope shifts ; Solvent effects ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of all possible indoles substituted with one, two or three methyl groups on the pyrrole ring were assigned from heteronuclear two-dimensional 13C/1H contour plots and homonuclear hydrogen-hydrogen decoupling experiments at a specific concentration of 0.83 M in CDCl3 and in DMSO-d6. The results confirm controversial assignments for some compounds, and provide the assignments for those compounds not previously studied by this technique. In addition, deuterium/hydrogen NMR isotope effect on 13C chemical shifts (DHIECS) for indoles, wherein the labile NH was partially exchanged to ND, are reported. In this way DHIECS values over two, three, four and five bonds were measured. The results in each solvent are discussed in terms of the number of bonds between the exchanged hydrogen and the observed carbon, and also according to their geometric dependence. This provides some evidence of the vibrational origin of the DHIECS.
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  • 33
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    Organic Magnetic Resonance 26 (1988), S. 671-674 
    ISSN: 0749-1581
    Keywords: Conformational analysis ; Cyclic sulphates ; 13C NMR ; 17O NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational analysis of cyclic sulphates with 5-7-membered rings is discussed on the basis of 13C and 17O NMR spectroscopic studies.
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  • 34
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    Organic Magnetic Resonance 26 (1988), S. 687-692 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Configurational assignment ; β-Hydroxysulphoxides ; 2-Alkylsulphinyl-1-arylethanol ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The relative configurations of erythro- and threo-2-alkylsulphinyl-1-phenyl(or 2-thiophen or 2-furyl)ethanol have been correlated with 13C NMR data. A general rule for determining the configuration of this type of compound is presented.
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  • 35
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    Organic Magnetic Resonance 26 (1988), S. 693-700 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; Benzomorphans ; 2D NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The high-frequency 1 and 13C NMR spectra (at 500 and 75.47 MHz, respectively) of metazocine (MTZ) fumarate, pentazocine (PTZ) and cyclazocine (CLZ) hydrochlorides in 2H2O solution were recorded and analysed with the aid of both homonuclear 1H—1H and heteronuclear 13C—1H chemical shift correlation experiments. At neutral pH all compounds were found to be configurationally heterogeneous, with the N-equatorial isomer more populated than the N-axial isomer (ratio ca 80:20). The low-intensity peaks of the superimposed spectral pattern of the less populated isomer were also assigned on correlative grounds in both the 1H and 13C NMR spectra of MTZ, PTZ and CLZ. The occurrence of distinct spectra for the two configurational isomers was diagnostic of a ‘slow’ exchange process on the NMR time-scale at the field frequencies employed for the experiments, thus suggesting a high-energy barrier to interconversion. The experimental proton-proton coupling constants measured for the N-equatorial form of MTZ, PTZ and CLZ were consistent with a chair conformation of the piperdinic ring in all compounds. The distinct relative agonist-antagonist potencies of the drugs investigated could therefore not be correlated with the above-described configurational and conformational features.
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  • 36
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    Organic Magnetic Resonance 26 (1988), S. 497-500 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 119Sn NMR ; Organotin derivatives ; Karplus relationship ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Multinuclear (1H, 13C, 119Sn) NMR data are presented for a series of compounds of the type XMe2SnCHRCHR'CO2Me (X = Me, Cl; R, R' = Me, Ph). Values of 3J(H, H), 3J(Sn, H) and 3J(Sn, C) were used to assign the preferred conformations of these compounds and at the same time to test the empirical relationships proposed previously for 3J(Sn, C) and (indirectly) 3J(Sn, H); the validity of these relationships was confirmed.
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  • 37
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; 13C—1H coupling constants ; Azide-tetrazole tautomerism ; Azidobenzene ; Tetrazolo[1,5-a]pyridine ; Azidopyrimidines ; Ditetrazolo[1,5-a: 1′,5′-c]pyrimidine ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton-coupled 13C NMR and 1H NMR spectra of azidobenzene, tetrazolo[1,5-a]pyridine, 2-azidopyrimidine and tetrazolo[1,5-a]pyrimidine in different solvents have been analysed, and criteria for using the NMR spectral parameters (especially the 13C-1H coupling constants) for tautomeric structure determination have been elaborated. The efficiency of these criteria has been demonstrated in studies of azide--tetrazole equilibria in 2,4- and 4,6-diazidopyrimidines. The ditetrazolo tautomeric form of 2,4-diazidopyrimidine has been found in polar solvents.
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  • 38
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    Organic Magnetic Resonance 26 (1988), S. 73-77 
    ISSN: 0749-1581
    Keywords: N,N-Diethylacetamides ; α-Heterosubstituted amides ; 13C NMR ; Substituent effects ; trans-γ and -δ effects ; cis-γ and -δ effects ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbon-13 NMR chemical shifts of a series of α-monosubstituted N,N-diethylacetamides [YCH2C(O)NEt2, Y = Me, Cl, Br, I, OMe, SMe, and NMe2] are reported. The α-methylene and carbonyl carbon chemical shifts are correlated with the Pauling electronegativities (Ep) and Charton's localized electrical parameters (σL), respectively. The non-equivalence of the chemical shifts for the syn and anti-N-alkyl carbon atoms are attributed to the electric field and steric compression effects and also to the YCH2cis and trans-γ-effects.
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  • 39
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    Organic Magnetic Resonance 26 (1988), S. 89-91 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 2(5H)-Furanones ; 3(2H)-Furanones ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of a series of novel 2(5H)-furanones were studied. The assignments of the carbon resonances were made on the basis of chemical shifts, long-range carbon-hydrogen couplings, intarnal comparison and known reference sources.
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  • 40
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    Organic Magnetic Resonance 26 (1988), S. 111-116 
    ISSN: 0749-1581
    Keywords: Diphenylmercury ; Bis(o-tolyl)mercury ; Bis(m-tolyl)mercury ; Phenyl(o-tolyl)mercury ; 13C NMR ; T1 values ; Rotation barriers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Barriers to rotation about the preferred axis, C-4—Hg—C-4′, were determined for diphenyl-, bis(o-tolyl)- and bis(m-tolyl)-mercury from 13C T1 relaxation times as a function of temperature in DMSO and in 1,1,2,2-tetrachloroethane-CCl4. Based on results for the unsymmetrical compound phenyl(o-tolyl)mercury, the rotation about the preferred axis is interpreted as rotation about the carbon-mercury bond. The average barrier to internal rotation of 3.6 ± 0.6 kcal mol-1 is constant as a function of both methyl substitution and coordinating and non-coordinating solvents.
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  • 41
    ISSN: 0749-1581
    Keywords: 13C NMR ; azoles ; N-substituent effects in azoles ; metallotropy ; additive ; 13C NMR models ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C chemical shifts and a large collection of coupling constants have been measured for 169 N-substituted azoles with no other substituents on the ring. Simple additive models have been used to discuss both the chemical shifts and the coupling constants. The chemical shift of the substituent depends on the nature of the azole which can, accordingly, be classified into three to six families. Some structural problems (ring-chain isomerism of 1-trifluoromethylsulphonyl-1,2,3-triazole, silylotropy and stannotropy) are also discussed.
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  • 42
    ISSN: 0749-1581
    Keywords: 13C NMR ; Chemical shifts ; Crown ethers ; Conformations ; Complexes ; Naphthalene ; Sodium ion ; Potassium ion ; Rubidium ion ; Cesium ion ; Binding constants ; Alkali metal cations ; Complexation constants ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR studies of alkali metal cation complexation by six related crown ethers are described. The crown ethers (and ions studied) were 2,3-naphtho-20-crown-6 (Na+, K+, Rb+, Cs+), 2,3-naphtho-17-crown-5 (Na+, K+, Rb+, Cs+), 2,3-naphtho-14-crown-4 (Na+, K+, Rb+, Cs+), 1,8-naphtho-21-crown-6 (Na+, K+, Rb+, Cs+), 1,8-naphtho-18-crown-5 (Na+, K+, Rb+, Cs+) and 1,5-naphtho-22-crown-6 (K+, Rb+, Cs+). For each crown ethercation combination, 13C NMR spectra were obtained for a number of different ion concentrations in CD3OD. Data were analysed by a non-linear least-squares treatment to give complexation constants and chemical shifts that would result at the limit of complete 1:1 complexation. Analyses of the limiting chemical shifts for a number of carbons indicate regular, cation-dependent trends (for Cs+ through Na+). Deviations from these trends are interpreted as reflecting differences in conformations of crown ether-cation complexes. Conformational differences between cation complexes that occur near the point of naphthalene attachment cause deviations from the trend in the aromatic carbon chemical shifts, while conformational differences further from the naphthalene cause trend deviations only in the crown ether carbon chemical shifts.
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  • 43
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    Organic Magnetic Resonance 26 (1988), S. 347-350 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Chemical shift assignments ; Carbazole derivatives ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR chemical shift assignments have been made for a series of 1-substituted carbazoles, 8-substituted 1,2,3,4-tetra-hydrocarbazoles, 1-substituted benzo[a]carbazoles and 6-substituted dibenzo-[c,g]carbazoles. Single examples were examined of other classes of substituted carbazoles: 3-butylcarbazole and its tetrahydro precursor 6-butyl-1,2,3,4-tetra-hydrocarbazole, 8-butyl- and 8,10-diethylbenzo[a]carbazoles and their 5,6-dihydro precursors, dibenzo[a,i]carbazole and its 5,6,7,8-tetrahydro precursor, benzo[c]carbazole and its 6-chloro derivatives and 5,6-dihydrobenzo[c]carbazole and 5,6,8,9-tetrahydrodibenzo[c,g]carbazole and their N-methyl derivatives. In addition, the N-(1-pyrrolidinomethyl) derivatives of carbazole, 1,2,3,4-tetrahydrocarbazole, benzo[c]carbazole and dibenzo[c,g] carbazole were also studied.
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  • 44
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    Organic Magnetic Resonance 26 (1988), S. 533-535 
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1-(Trifluoromethyl)dihydronaphthalenes ; 1-(Trifluoromethyl)tetrahydronaphthalenes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR data for variously functionalized and substituted 1-CF3-tetrahydronaphthalenes are reported. A complete assignment of the chemical shifts has been achieved.
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  • 45
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    Organic Magnetic Resonance 26 (1988), S. 626-628 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Hexa-2,4-diynes ; Sulphones Sulphoxides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR data for 1,6-bis derivatives of hexa-2,4-diynes are reported. Introduction of a sulphone or sulphoxide moiety at C-1, C-6 in place of sulphide, ether or amino groups caused a 6-7 ppm upfield shift (β effect) for the C-2, C-5 carbons and a 3-4 ppm downfield shift (y effect) for the C-3, C-4 carbons.
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  • 46
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; ASIS ; 1H-{1H} ; NOE ; DEPT ; INEPT ; Configuration determination ; Conformation study ; Cephalosporins ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of known and novel 2-methylenecephem derivatives were prepared and their reactions with diazomethane, phenyldiazomethane and diphenyldiazomethane were studied. The initially formed 1-pyrazolino derivatives easily underwent spontaneous loss of nitrogen, leading to 2-spirocyclopropylcephems. The two reaction products, formed in a 3:1 to 8:1 ratio on addition of diphenyldiazomethane, were separated by column chromatography and distinguished by their 1H and 13C NMR spectra. The 1H NMR spectra did not exclude the possibility of 1-pyrazoline formation, but elemental analysis and 13C data corroborated the previous assumption that loss of nitrogen took place, even in those cases when it did not occur during the reaction.
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  • 47
    ISSN: 0749-1581
    Keywords: 13C NMR ; Proton-proton interaction ; Glycosides ; Disaccharides ; Configuration ; Conformation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Basic stereochemical factors have been revealed which affect the 13C chemical shifts in glycosides with a chiral cyclohexane-type aglycone and in disaccharides with a pyranosidic aglycone. The effects of glycosylation depend on the configuration of the anomeric centre of the glycosylating sugar residue (glycone) and on the relative absolute configuration of the glycone and aglycone. When at least one of the carbons of the aglycone, adjacent to the glycosylated carbon, bears an equatorial proton, this dependence is well accounted for by a strengthening or weakening of the spatial interaction between the protons of the glycone and aglycone, caused by a change in the conformation around the glycosidic linkage. Regularities in the glycosylation effects for disaccharides are generalized for various modes of substitution and different general configurations of the pyranosidic aglycones. Simple rules have been formulated for the prediction of the magnitudes of the glycosylation effects which can be used for the determination of some unknown structural elements in glycosides and disaccharides, in particular the absolute configuration of one of the constituent sugars.
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  • 48
    ISSN: 0749-1581
    Keywords: 13C NMR ; Spin-lattice relaxation data ; Tropine ; Pseudotropine ; Rotational diffusion ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Models for isotropic, axially symmetric and fully anisotropic overall rotational diffusion with single diffusional or three-state internal motion are reviewed or derived and applied to 13C spin-lattice relaxation data for the N-methyl groups of tropine and pseudotropine. The results are compared. Complete equations containing the dependence on the equilibrium positions are given for the three-state jump models. Despite the considerable approximations which these models imply, they are able to predict the expected features of the internal N-methyl group motion in tropine and pseudotropine: hindered three-state jumping, which is of the same rate for tropine and pseudotropine and which is moderately independent of concentration and the model for overall motion. Although the nitrogen inversion in these compounds is slow compared with methyl rotation, and does not affect the relaxation, the equations are also derived for double internal motion where the internal rotation axis jumps between two non-equivalent sites having an arbitrary but fixed orientation within the molecule, and where the innermost internal motion is diffusional or jumpwise as in single internal motion. Some considerations regarding the units of the rotational diffusion constants, errors in T1 measurements, and the reduction of the equations for fully anisotropic overall motion to equations for axially symmetric and, further, for isotropic overall motion are presented.
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  • 49
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    Organic Magnetic Resonance 24 (1986), S. 1093-1094 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Aniline derivatives ; Benzothiazolidines ; 2,3-Dihydroperimidines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR chemcical shifts of 23 aniline and 1,8-diaminonaphthalene derivatives are reported; the parent compounds are also included for purposes of comparison.
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  • 50
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    Organic Magnetic Resonance 24 (1986), S. 772-776 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Carbon-carbon coupling constants ; SEMINA-1 technique ; Tautomerism ; Phenylazonaphthols ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbon-carbon coupling constants of 1-phenylazo-2-naphthol and 2-phenylazo-1-naphthol have been measured with the SEMINA-1 pulse sequence. The carbon-carbon couplings provide an unambiguous assignment of the 13C spectra. The magnitudes of the carbon-carbon coupling constants are discussed in relation to the tautomeric nature of the compound. Substituent effects on couplings are also considered.
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  • 51
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    Organic Magnetic Resonance 24 (1986), S. 768-771 
    ISSN: 0749-1581
    Keywords: Solid-state ; 13C NMR ; Aspirin ; Drugs ; Polymorphism ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Natural abundance 13C NMR spectra of different crystal habits of pure aspirin and several aspirin tablets in the solid state have been measured by using the combined techniques of high-power decoupling, cross-polarization and magic angle spinning. Solid-state NMR of aspirin had excellent sensitivity compared with liquid-state NMR, and the carbon signals were assigned using a modified pulse sequence to detect non-protonated carbons. The solid-state 13C NMR spectra of two crystalline forms of aspirin were identical, suggesting that the origin of their difference is not polymorphic.The solid-state 13C NMR spectra of several commercial aspirin tablets, some of them containing buffer components, indicated that there were no interactions among the aspirin and the buffer components; only after dissolving the tablets and lyophilization did the 13C NMR spectra of the dry lyophilized powders show strong interactions between aspirin and the buffer components.
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  • 52
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    Organic Magnetic Resonance 24 (1986), S. 465-479 
    ISSN: 0749-1581
    Keywords: β-Lactam antibiotics ; Penicillin ; Cephalosporin ; 13C NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR features of most β-lactam antibiotics of the penicillin and cephalosporin groups in clinical use are presented and reviewed. Data on precursor and breakdown products are included in the survey, with particular reference to benzylpenicillin. Penicillin and cephalosporin spectra are discussed, and points of similarity and difference emphasized. The potential of the data for solving problems of analysis, stability, degradation and biological structure-activity relationships is summarized.
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  • 53
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; condensed tetrahydroquinoxalines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H and 13C NMR spectra of tetrahydroquinoxalines condensed with pyridazine, pyrazine, oxazine, oxadiazine, thiadiazine or triazine rings have been measured in DMSO-d6 solution. The effects of six-membered heterocycles on 1H and 13C chemical shifts and the values of one-bond 1J(CH) and vicinal 3J(HH) coupling constants for the ring junction fragment are considered. The differences between the 1H and 13C spectral parameters of tetrahydroquinoxalines annelated with five- or six-membered heterocycles with the same set of heteroatoms attached to the ring junction carbons are also discussed.
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  • 54
    ISSN: 0749-1581
    Keywords: 13C NMR ; 1H NMR ; Ni-Pd-Pt series ; Ni-Pd-Pt substituent effects ; Ni/Pd/Pt-induced paramagnetic shifts ; M(PEt3)2X substituents ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C and proton NMR spectra of several arylpalladium and some arylnickel and arylplatinum complexes have been compared. The Ni(PEt3)2X and Pd(PEt3)2X substituents induce a paramagnetic shift of Cipso (of the phenyl ring) which is much larger than that induced by Pt(PEt3)2X. However, there are no significant differences along the Ni/Pd/Pt series for the ortho, meta and para positions. For the six compounds of general formula trans-[ArPdBr(PEt3)2] reported here, the mean Δ(δ)C values induced on the ArH by the introduction of the PdBr(PEt3)2 substituent are found to be 26.9 (Cipso), 7.2 (Cortho), -1.1 (Cmeta), -5.5 (Cpara), -0.03 (Hortho), -0.28 (Hmeta) and -0.38 ppm (Hpara).
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  • 55
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    Organic Magnetic Resonance 24 (1986), S. 951-953 
    ISSN: 0749-1581
    Keywords: Carbon multiplicities ; 13C NMR ; Double echo sequence ; Gated decoupling ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simple pulse sequence, based on a double 13C echo and off gated proton decoupling, is shown to yield four subspectra (C, CH, CH2 and CH3) from linear combinations of four different experiments. This procedure has two advantages: (1) experimental simplicity, keeping instrumental adjustments to a minimum and (2) acquisition of the four experiments under identical lengths of the evolution period, thus eliminating any spurious effects due to transverse relaxation.
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  • 56
    ISSN: 0749-1581
    Keywords: 13C NMR ; 15N NMR ; Sodium tetrazolates ; tetrazoles ; bitetrazoles ; cobalt(III)tetrazole complexes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Natural abundance 13C and 15N nuclear magnetic resonance studies have been carried out on a series of sodium tetrazolate salts, 1,5- and 2,5-disubstituted tetrazoles, bitetrazoles, and cobalt(III) tetrazolate complexes of the type (PBu3n)Co(DH)2(5-R-tetrazolate), where DH is the monoanion of dimethylglyoxime. The 15N chemical shifts have been analysed with respect to structure, substituent effects, electron density as determined by molecular orbital calculations, Brønsted acidity, Lewis basicity and nucleophilicity of the nitrogen atoms in the ambidentate tetrazoles.
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  • 57
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 879-882 
    ISSN: 0749-1581
    Keywords: Flavones ; Apigenin ; 1H NMR ; 13C NMR ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The assignment of some 1H and 13C NMR chemical shifts of apigenin have been uncertain and even contradictory. A reinvestigation with recent NMR techniques has led to a new set of 13C NMR parameters and confirmed the accepted 1H NMR data.
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  • 58
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 259-262 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Broad band decoupling ; WALTZ-16 ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The interfacing of a circuit to generate WALTZ-16 decoupling pulse trains with a JEOL FX series NMR spectrometer is possible for any instrument which has a 0°/180° phase shifter control line. The use of the decoupler gives a reduction in sample heating and line width improvements.
    Additional Material: 4 Ill.
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  • 59
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 15N NMR ; 2-methylthio-(glyco)oxazolines ; ring size ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A facile synthesis of 2-methylthio-(glyco)oxazoline derivatives has been developed which involves methylation of 2-thiono-(glyco)oxazolidines prepared by condensation of aldoses with thiocyanate ion. The synthesis has been applied to the preparation of six 2-methylthiooxazoline derivatives in the pentose series and six derivatives in the hexose series. For several sugars, both pyranoid and furanoid forms were isolated, and the use of either 13C- or 15N-labeled thiocyanates yielded either 2-13C-labeled or 3-15N-labeled derivatives. The structures of the products have been studied by 1H, 13C and 15N NMR spectroscopy and by electron-impact and field desorption mass spectrometry. Multinuclear chemical shift correlations and analyses of fragmentation pathways have facilitated the assignment of ring size in the 2-methylthio-(glyco)oxazoline derivatives.
    Additional Material: 4 Ill.
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  • 60
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 1008-1012 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Ring forms of digitoxose ; DEPT Spectrum editing ; 2D CH Chemical shift correlation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C chemical shifts of the four isomeric ring forms of D-digitoxose in dimethyl sulfoxide-d6 solution have been assigned completely by DEPT 13C NMR spectrum editing and two-dimensional carbon-proton chemical shift correlation spectroscopy. The 13C chemical shifts are discussed in terms of their dependence on ring size and on anomeric configuration. The equilibrated mixture of four ring forms of D-digitoxose in dimethyl sulfoxide-d6 solution has been analysed quantitatively by 13C NMR spectroscopy, and the results compared with those obtained previously by 1H NMR.
    Additional Material: 4 Ill.
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  • 61
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 1014-1016 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 4-n-alkyl-4′-cyanobiphenyls 4-n-alkyloxy-4′-cyanobiphenyls ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C and 1H NMR spectra of two series of mesogenic compounds dissolved in CDCl3 were studied. The compounds are 4-n-alkyl-4′-cyanobiphenyls and 4-n-alkyloxy-4′-cyanobiphenyls, with the alkyl group ranging from pentyl to octyl. 13C and 1H chemical shifts and 13C-1H scalar coupling constants are tabulated.
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  • 62
    ISSN: 0749-1581
    Keywords: 1,3-dioxolane derivatives ; 13C NMR ; Shift parameters ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 13C NMR spectra of 24 1,3-dioxolane derivatives are reported in an attempt to propose parameters for the C-2, C-4 and C-5 shifts from the 2-Me and 4-Me substituents, based on the ring stereochemistry. These parameters are obtained from simultaneous equations, and clearly agree with those calculated by the use of pattern molecules. The calculated parameter for the C-4 shift due to a 2-Me group differs notably from that proposed by other workers.
    Additional Material: 4 Tab.
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  • 63
    ISSN: 0749-1581
    Keywords: 13C NMR ; Diterpenes ; ent-Beyeranes ; ent-Beyer-15-enes ; Bicyclo[3.2.1]octanes ; Substituent effects ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed analysis of the 13C NMR spectra of 39 isomeric ent-beyer-15-enes and ent-beyeranes functionalized at C-7, C-14, C-15 and C-16 has been performed. This diterpenic skeleton is a good example of a semirigid bicyclo[3.2.1]octane system. The sensitivity of 13C shielding to the stereochemical environment, particularly in polyfunctional compounds, has been confirmed. In some cases the ent-beyer-15-enes and ent-beyeranes show similar behaviour to that of similarly functionalized bicyclo[3.2.1]octane derivatives, but in other cases the shielding effects are very different. The compounds studied are a good model for the evaluation of shielding effects in exo/endo isomers of strained and rigid carbocyclic compounds.
    Additional Material: 12 Tab.
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  • 64
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 995-998 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Spectral simulation ; Substituted alkanes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The empirical prediction of 13C NMR chemical shifts using the Lindeman-Adams rules and substituent chemical shift parameters is a useful aid for the chemist in the interpretation of spectra. The program Alkanes, written in Basic for a desk-top microcomputer, automates the chemical shift estimation.
    Additional Material: 3 Ill.
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  • 65
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 1073-1076 
    ISSN: 0749-1581
    Keywords: 13C NMR ; deuterium isotope effects ; methylbenzenes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complete series of all possible benzenes bearing one deuterium atom and one to five methyl groups was synthesized. The deuterium isotope effects on the carbon chemical shifts of the aromatic and aliphatic carbon atoms were measured and shown to obey an empirical increment system. The isotope effects over one bond correlate with the C,H spin coupling constants.
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  • 66
    Electronic Resource
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    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 24 (1986), S. 612-615 
    ISSN: 0749-1581
    Keywords: Lanthanide-induced shifts1 ; 13C NMR ; Conformational Analysis ; Statistical Models ; Fatty Acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conformational analysis of short polymer chains involves the use of statistical models, and their predictions must be checked against experimental information. Ytterbium-induced shifts in the 13C NMR spectra of fatty acids provide a non-perturbing, straightforward method of simultaneously obtaining positional information about all the carbon atoms up to nine bonds away from the comuplexation point. Experimental results for saturated and unsaturated C-18 fatty acids are compared with the predictions of a restricted isomeric states (RIS) model.
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  • 67
    ISSN: 0749-1581
    Keywords: 13C NMR ; Carbons ; α to Carbonyl Group ; cis-Decalins ; cis-Decalones ; cis-Hydrindanones ; 13α,14α- and 13β,14β-Steroids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new 13C NMR method based on solvent effects allows the identification of carbon atoms α to a carbonyl group. With a simple change in solvent from CDCl3 to CDCI3-dioxane (1:4), the 13C absorption for all earbons except those α to the carbonyl group in the compounds under study were displaced to lower field by 0.2-0.5 ppm. The α-carbon absorptions either remained unchanged or were shifted to higher field by ca 0.1 ppm. The validity of the method has been checked on compounds with fully assigned 13C NMR spectra (trans-decalones and steroids). Moreover, no modification of these solvent shifts due to the presence of other common functional groups (double bond or OH) was observed. This new technique, together with existing ‘classical’ methods (‘off-resonance’ spectra, substituent effects) enables the complete interpretation of the 13 C NMR spectra of five cis-decalins and cis-decalones to be made. The spectra of three cis-hydrindanones which have not been previously described were also fully interpreted.The same method allows the complete spectral assignment of the 13C NMR spectra of six steroids of unnatural configuration in the 13α,14α- and 13β,14β-androstane series, for which no data were previously available.
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