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  • Organic Chemistry  (9,519)
  • 1995-1999  (2,690)
  • 1980-1984  (3,406)
  • 1975-1979  (3,423)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 964-972 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Investigations on the Thermal Decomposition of n-Dodecylcyclopentane in the Gas PhaseIn the thermal decomposition of n-dodecylcyclopentane at 670 and 750°C in a laboratory tubular reactor mixtures of hydrogen and 57 and 113 hydrocarbons respectively are formed. The mixtures have been analyzed and identified by capillary gas chromatography and by mass spectrometry. The distribution of the reaction products is used for mechanistic discussions.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 66-74 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Kinetic Investigations of the Pyrolysis of Mono-n-alkyl-cyclohexanesThe thermal decomposition of cyclohexane and six mono-n-alkylcyclohexanes was studied kinetically in a metallic laboratory tubular reactor at 650 to 850°C and atmospheric pressure.Kinetic parameters were found to be a function of length of the alkylic side chain. A comparison with analogous parameters of n-paraffins and the unsubstituted cyclohexane allowed the conclusion that C—C-scission in the alkylic chain is the initial reaction in pyrolysis of n-alkylcyclohexanes followed by radical attacks to all C—H-bonds of the feed molecules.
    Additional Material: 4 Ill.
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  • 3
    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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  • 4
    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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  • 5
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The conjugate addition of the chiral, non-racemic alkoxy-enolates 5 and 6 to nitroolefins furnishes the hydroxynitroesters 7-13, which are catalytically hydrogenated to give the lactams 14-18. The configuration of adduct 7 from nitroethylene was elucidated by NMR. analysis of the acetal 20 derived from 7. The assignment establishes that the reaction follows the stereochemical rule of attack depicted in 21 and previously deduced for other electrophiles, i.e. formation of erythro-products of type 3b and 4b. No stereocontrol was found at the newly formed chiral centers in α- and β-position to the NO2 group of 8-12.
    Additional Material: 1 Tab.
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  • 6
    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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  • 7
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The protonation and deprotonation rates of the coordinated amide groups in the Cu2+-complexes of 1,8-diamino-3,6-diaza-2,7-octanedione (DED = L) have been studied by stopped-flow techniques. Starting at low pH from Cu2+ and DED the dimeric Cu2L24+-complex, fully formed within the mixing time of the stopped-flow instrument, reacts in two consecutive steps to yield the final product CuLH-2. The rate constants of the forward and backward reactions have been determined and are given in Table 1. The intermediate was identified as Cu2L2H-22+ by measuring its VIS.-absorption spectrum.The rate constants for the interconversion of the amide groups from the O- to the N-coordinated form in the Cu2+-complexes of DED, 2,10-dioxo-1, 4, 8, 11 tetraazaundecane (DANA) and triglycine (TRIGLY) are compared with each other. It is shown that these rate constants are similar, no matter whether the amide group is terminal or internal as long as the rotation is easily possible as is the case in the dimeric species Cu2L24+ and Cu2L2H-22+. However, for CuLH-2 the inter-conversion only takes place after opening of one of the chelate rings in a rapid protonation preequilibrium.
    Additional Material: 5 Ill.
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  • 8
    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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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 1011-1015 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H- and 13C-N.M.R. Investigations of N-Acyl-imino-dithiocarbonic-S,S-dimethylester
    Additional Material: 3 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1982 (1982), S. 1366-1374 
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of cis- and trans-Enynes in the Class of 12- and 15-membered Ring SystemsSynthesis of (E)-1-cyclododecen-3-yne (E-2a) leads to the isolation of the first trans-enyne with geometrical ring strain. E-2a isomerizes thermally to give the Z-configuration Z-2a in a very smooth reaction. For systematical investigations the 15-membered ring enynes E-5a and Z-5a were generated. They behave like openchained 1,3-enynes.
    Notes: Die Synthese von (E)-1-Cyclododecen-3-in (E-2a) führt zur Isolierung des ersten trans-Enins mit geometrischer Ringspannung. E-2a wandelt sich thermisch leicht in die Z-Konfiguration Z-2a um. Zur systematischen Untersuchung werden die 15-Ring-Enine E-5a und Z-5a hergestellt. Sie verhalten sich wie offenkettige 1,3-Enine.
    Additional Material: 1 Ill.
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