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Volumn 63, Issue 21, 1998, Pages 7306-7310

Studies on the asymmetric oxidation of ester derivatives of 1,3-dithiane-2-carboxylates. asymmetric synthesis of trans-1,3-dithiane 1,3-dioxide

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EID: 0000308238     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9807971     Document Type: Article
Times cited : (30)

References (51)
  • 3
    • 0001097869 scopus 로고
    • Trost, B. M., Fleming, I., Ed.; Pergamon Press: Oxford
    • Solladie, G. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Ed.; Pergamon Press: Oxford, 1991; Vol. 6, pp 133-170.
    • (1991) Comprehensive Organic Synthesis , vol.6 , pp. 133-170
    • Solladie, G.1
  • 37
    • 0001272894 scopus 로고
    • Paquette, L. O., Ed.; Wiley: New York
    • de Lucchi, O.; Miotti, V.; Modena, G. In Organic Reactions; Paquette, L. O., Ed.; Wiley: New York, 1991; Vol. 40, pp 157-405.
    • (1991) Organic Reactions , vol.40 , pp. 157-405
    • De Lucchi, O.1    Miotti, V.2    Modena, G.3
  • 40
    • 0041968335 scopus 로고
    • Page has oxidized the t-Bu ester and reported an ee of 54% for the product following hydrolysis and decarboxylation: Page, P. C. B.; Wilkes, R. D.; Barkley, J. V.; Witty, M. J. Synlett 1994, 547-550. We cannot account for this discrepancy.
    • (1994) Synlett , pp. 547-550
    • Page, P.C.B.1    Wilkes, R.D.2    Barkley, J.V.3    Witty, M.J.4
  • 41
    • 33744839639 scopus 로고    scopus 로고
    • Kagan has reported the absolute configuration of 8 (see ref 29)
    • Kagan has reported the absolute configuration of 8 (see ref 29).
  • 47
    • 33744852510 scopus 로고    scopus 로고
    • note
    • It is possible that the preexisting stereocenter influenced the outcome of the second oxidation. However, we have never observed any reagent control in this process; the second oxidation does not seem to be affected by the first.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.