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  • Organic Chemistry  (6,113)
  • 1995-1999  (2,690)
  • 1975-1979  (3,423)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 321 (1979), S. 1000-1006 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Model Calculations on the Counterion Effect in the Cationic Polymerization; Decay of the Mixed Halogenoantimonates SbCl5Br- and SbClBr5-The decay of the halogenoantimonates SbCl5Br- and SbClBr5- according to SbCl5Br- → SbCl5 + Br- resp. SbCl4Br + Cl- and SbClBr5- → SbBr5 + Cl- resp. SbClBr4 + Br- has been investigated by the quantum-chemical CNDO/2 method including geometry optimization. The calculations show that the dissociation of the Sb—Cl bond needs more energy (7,8 kcal/mol) than the dissociation of the Sb—Br bond.Dissociation of the complex anions is facilitated with increasing Br content.
    Additional Material: 4 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Chirality 10 (1998), S. 362-363 
    ISSN: 0899-0042
    Keywords: Jacobsen's catalyst ; enantiomeric purity determination ; chiral HPLC ; cyclodextrin chiral stationary phases ; enantioseparation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A HPLC method is described for the chiral analysis of the commercially available Jacobsen's catalyst. A hydroxypropyl β-cyclodextrin stationary phase was used in conjunction with a nonaqueous, polar-organic mobile phase. The method can be applied to control the enantiomeric purity of the catalyst, which is of great importance for quality control of that product. High accuracy in the determination of trace levels of the unwanted enantiomer in the presence of large amounts of the desired enantiomer is demonstrated. Chirality 10:362-363, 1998. © 1998 Wiley-Liss, Inc.
    Additional Material: 1 Ill.
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  • 3
    ISSN: 0947-3440
    Keywords: Bond cleavage, C-C kinetics of ; Radicals, stability of ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Products and kinetics of the homolytic thermolyses reactions of the three tertiary amides 6a-c of 2,3,3-triphenylpropanoic acid were studied in solution. The steric effects on the C-C bond homolysis processes were evaluated from MM2 calculations. Taking this into account, we deduced radical stabilization enthalpies RSE for the α-carbamoylbenzyl radicals 3a-c from the activation enthalpies ΔH≠ [RSE (kcal/mol): 8.3 ± 2.8 (3a), 10.3 ± 2.7 (3b), 9.0 ± 2.2 (3c)].
    Additional Material: 5 Tab.
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complexation of 1-methyl-2-hydroxymethyl-imidazole (L) with Cu(I) and Cu(II) has been studied in aqueous acetonitrile (AN). Cu(I) forms three complexes, Cu(AN)L+, CuL2+, and Cu(AN)H-1L, with stability constants logK(Cu(AN)+ + L ⇌ Cu(AN)L+) = 4.60 ± 0.02, logβ2 = 11.31 ± 0.04, and logK(Cu(AN)H-1L+H+ ⇌ Cu(AN)L+) = 10.43 ± 0.08 in 0.15M AN. The main species for Cu(II) are CuL2+, CuH-1L+, CuH-1L2+, and CuH-2L2.The autoxidation of CuL2+ was followed with an oxygen sensor and spectrophotometrically. Competition between the formation of superoxide in a one-electron reduction of O2 and a path leading to H2O2 via binuclear (CuL2)2O22+ was inferred from the rate law \documentclass{article}\pagestyle{empty}\begin{document}$${{ - {\rm d}\left[{{\rm O}_2 } \right]} \mathord{\left/ {\vphantom {{ - {\rm d}\left[{{\rm O}_2 } \right]} {{\rm dt}}}} \right. \kern-\nulldelimiterspace} {{\rm dt}}} = \left[{{\rm CuL}_2^ + } \right]^2 \left[{{\rm O}_2 } \right]\left({\frac{{k_{\rm a} }}{{1 + k_{\rm b} \left[{{\rm CuL}^ + } \right]}} + \frac{{k_{\rm c} \left[{\rm L} \right] + k_{\rm d} + {{\left({{{k_{\rm f} } \mathord{\left/ {\vphantom {{k_{\rm f} } {\left[{\rm L} \right]}}} \right. \kern-\nulldelimiterspace} {\left[{\rm L} \right]}} + k_{\rm g} + k_{\rm h} \left[{\rm L} \right]} \right)} \mathord{\left/ {\vphantom {{\left({{{k_{\rm f} } \mathord{\left/ {\vphantom {{k_{\rm f} } {\left[{\rm L} \right]}}} \right. \kern-\nulldelimiterspace} {\left[{\rm L} \right]}} + k_{\rm g} + k_{\rm h} \left[{\rm L} \right]} \right)} {\left[{{\rm H}^ + } \right]}}} \right. \kern-\nulldelimiterspace} {\left[{{\rm H}^ + } \right]}}}}{{\left[{{\rm CuL}_2 ^ + } \right] + k_{\rm e} \left[{{\rm Cu}\left({{\rm II}} \right)} \right]_{{\rm tot}} }}} \right)$$\end{document} with ka = (2.31 ± 0.12) · 104M-2S-1, kb = (1.0 ± 0.2) · 103M-1, kc = (2.85 ± 0.07) · 102M-2S-1, kd = 3.89 ± 0.14M-1S-1, ke = 0.112 ± 0.004, kf = (2.06 ± 0.24) · 10-10M S-1, kg = (1.35 ± 0.07) · 10-7 S-1, and kh = (6.8 ± 1.4) · 10-7M-1 S-1.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 60 (1977), S. 1845-1860 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thallium compounds as catalysts for transesterifications and ester exchange reactionsThe transesterification of di-, tri- and tetracarboxylic alkyl esters with 2,3-epoxy-propanol was investigated in the presence of various metal compounds as catalysts. It was found that only thallium compounds catalyse the reactions under mild conditions without decomposition of 2,3-epoxypropanol. Many thallium compounds also proved to be very good catalysts for the reactions of 2,3-epoxypropanol with alkoxysilanes and the ester exchange reactions of di-, tri- and tetracarboxylic alkyl esters with 2,3-epoxypropyl-acetate.
    Additional Material: 5 Tab.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 58 (1975), S. 2261-2267 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The catalytic hydrogenation of α-mono- and bis-cyanoethylated aldiminesThe catalytic hydrogenation of α-mono- and -bis-cyanoethylated aldimines using nickel catalysts was studied. Piperidine derivatives are formed in intramolecular cyclization reactions. The hydrogenation products of α-bis-cyanoethylated ketones, the decahydro-1, 8-naphthyridines, are observed here only as by-products.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 58 (1975), S. 2247-2260 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The catalytic hydrogenation of aminalsThe catalytic hydrogenation of aminals, the bis-N-analogs of acetals, was investigated. 3-(γ-Aminopropyl)-piperidines are formed by the hydrogenolytic splitting of the C-N-bond of decahydro-1, 8-naphthyridines. The reaction is stereospecifically influenced by the catalyst used. Non cyclic aminals are hydrogenated in the same manner. The mass and NMR. Spectra of 3-(γ-aminopropyl)-piperidines are discussed.
    Additional Material: 6 Ill.
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  • 8
    ISSN: 0899-0042
    Keywords: (S)-ibuproxam ; enantiomers ; NSAID ; β-cyclodextrin ; solubilisation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (+)-(S)-Ibuproxam, a prodrug of (+)-(S)-ibuprofen, the pharmacologically active component of ibuprofen, was synthesized in order to minimize side effects (especially gastric irritation) and reduce effective dose. The low water solubility of (+)-(S)-ibuproxam, which prevents rapid dissolution and absorption from the gastrointestinal tract, was overcome by complexation with β-cyclodextrin and its derivatives. The inclusion complex formation was confirmed by differential scanning calorimetry (DSC), by 1H-NMR spectroscopy, and X-ray powder diffractometry. The physicochemical characteristics of ibuproxam were significantly improved by the complexation. © 1995 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 337 (1995), S. 156-158 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1996 (1996), S. 1511-1522 
    ISSN: 0947-3440
    Keywords: Aminolysis ; Esters ; Catalysis ; Calculations, ab initio ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Model systems for the reaction of amines with esters were investigated with ab initio methods. Ammonia and methylamine were used as models for primary amines, and formic acid, methyl acetate, phenyl acetate, and p-nitrophenyl acetate were chosen to represent typical esters. Geometry optimizations were performed for all systems with the HF/6-31G** method, and relative energies were evaluated by using MP2/6-31G** single-point energies. The lowest barriers are found for the reaction of methylamine with p-nitrophenyl acetate. Reaction occurs in this case according to a direct displacement pathway, in which all bond formation and breaking occurs in a single step. Complexation of the transition structures by dimethyl ether or dimethoxyethane leads to much the same changes as observed for variation of the leaving group. Based on the ab initio data a force field for the calculation of transition state-catalyst complexation was developed. This force field as well as ground state complexation energies were employed to predict catalytic activities for a number of polyethers, polyalcohols, and pyrans, which in part, were also investigated experimentally.
    Additional Material: 12 Ill.
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