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Volumn 7, Issue 11, 1996, Pages 3147-3152

An optimised in situ procedure for the oxazaborolidine catalysed enantioselective reduction of prochiral ketones

Author keywords

[No Author keywords available]

Indexed keywords

ALKANOL; BENZYL ALCOHOL DERIVATIVE;

EID: 0030575849     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00416-8     Document Type: Article
Times cited : (39)

References (23)
  • 1
    • 0000093375 scopus 로고
    • (Eds.: Trost, B. M; Fleming, I), Pergamon: Oxford
    • 1. (a) Nishizawa, M.; Noyori, R. In Comprehensive organic Synthesis vol.8 (Eds.: Trost, B. M; Fleming, I), Pergamon: Oxford, 1991, p.139.
    • (1991) Comprehensive Organic Synthesis , vol.8 , pp. 139
    • Nishizawa, M.1    Noyori, R.2
  • 12
    • 0001542996 scopus 로고
    • 6. A nice study dealing with the oxazaborolidine structure and enantioselectivity was reported recently. The investigation however fell short off prescribing "the ideal" structure of an oxazaborolidine structure. See: Quallich, G. J.; Blake, J. F.; Woodall, T. M. J. Am. Chem. Soc. 1994, 116, 8516.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 8516
    • Quallich, G.J.1    Blake, J.F.2    Woodall, T.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.