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Volumn 119, Issue 7, 1997, Pages 1565-1571

Chemical and biological oxidation of thiophene: Preparation and complete characterization of thiophene S-oxide dimers and evidence for thiophene S-oxide as an intermediate in thiophene metabolism in vivo and in vitro

Author keywords

[No Author keywords available]

Indexed keywords

DRUG METABOLITE; THIOPHENE;

EID: 0030991141     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja962466g     Document Type: Article
Times cited : (93)

References (50)
  • 1
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    • 0028693737 scopus 로고
    • August, J. T., Anders, M. W., Murad, F., Coyle, J. T., Eds.; Academic Press: New York
    • (b) Beaune, P.; Pessayre, D.; Dansette, P. M.; Mansuy, D.; Manns, M. In Advances in Pharmacology; August, J. T., Anders, M. W., Murad, F., Coyle, J. T., Eds.; Academic Press: New York, 1994, Vol. 30, pp 199-245.
    • (1994) Advances in Pharmacology , vol.30 , pp. 199-245
    • Beaune, P.1    Pessayre, D.2    Dansette, P.M.3    Mansuy, D.4    Manns, M.5
  • 13
    • 8244222096 scopus 로고    scopus 로고
    • Biological Reactive Intermediates
    • Greim, H., Jollow, D., Witmer, C., Snyder, R., Eds.; Plenum Press: New York. In press
    • (c) Mansuy, D.; Dansette, P. M. Biological Reactive Intermediates. In Advances in Experimental Medicinal Biology; Greim, H., Jollow, D., Witmer, C., Snyder, R., Eds.; Plenum Press: New York. In press.
    • Advances in Experimental Medicinal Biology
    • Mansuy, D.1    Dansette, P.M.2
  • 40
    • 8244247601 scopus 로고    scopus 로고
    • note
    • -3; 1379 independent reflections; R = 0.0720. Further details of the crystal structure of sesquioxide 5 are available on request from the Cambridge Crystallographic Data Centre by quoting the names of the authors and the journal citation.
  • 41
    • 0025259615 scopus 로고
    • and references cited therein
    • Since the nomenclature for the stereochemical prefixes of unsymetrically substituted brigde atoms is far from being unique, we prefer, with regard to earlier communications concerning Diels-Alder reactions of thiophene S-oxides, to name the configuration of the sulfoxide group syn when the oxygen atom directs toward the second ring and anti when it directs away from it. For a more detailed discussion, see: Macauley, J. B.; Fallis, A. G. J. Am. Chem. Soc. 1990, 112, 1136-1144 and references cited therein.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 1136-1144
    • Macauley, J.B.1    Fallis, A.G.2
  • 43
    • 8244248273 scopus 로고    scopus 로고
    • note
    • -3; 1291 independent reflections; R = 0.0433. Further details of the crystal structure of dimer 4a are available on request from the Cambridge Crystallographic Data Centre by quoting the names of the authors and the journal citation.
  • 48
    • 0003069097 scopus 로고
    • Raven Press: New York, Kroe Foundation Series; Chapters 12-14
    • Glutathione: Metabolism and Function; Arias, I. M.; Jakoby, W. B., Eds.; Raven Press: New York, 1976, Kroe Foundation Series; Vol. 6, Chapters 12-14, pp 189-232.
    • (1976) Glutathione: Metabolism and Function , vol.6 , pp. 189-232
    • Arias, I.M.1    Jakoby, W.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.