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Volumn 1, Issue 7, 1999, Pages 1119-1121

A practical stereoselective synthesis of chiral hydrobenzoins via asymmetric transfer hydrogenation of benzils

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Indexed keywords


EID: 0000759992     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol990226a     Document Type: Article
Times cited : (193)

References (36)
  • 1
  • 29
    • 0032499273 scopus 로고    scopus 로고
    • Asymmetric transfer hydrogenation of benzil by in situ generated diamine-based Ru catalyst using 2-propanol as a hydrogen source gave chiral hydrobenzoin with moderate enantiomeric purity (dl:meso = 31:69, 50% ee). Schwink, L.; Ireland, T.; Püntener, K.; Knochel, P. Tetrahedron: Asymmetry 1998, 9, 1143-1163.
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 1143-1163
    • Schwink, L.1    Ireland, T.2    Püntener, K.3    Knochel, P.4
  • 30
    • 0002923489 scopus 로고
    • and references therein
    • For computer-aided analysis of dynamic kinetic resolution, see: Noyori, R.; Tokunaga, M.; Kitamura, M. Bull. Chem. Soc. Jpn. 1995, 68, 36-56 and references therein.
    • (1995) Bull. Chem. Soc. Jpn. , vol.68 , pp. 36-56
    • Noyori, R.1    Tokunaga, M.2    Kitamura, M.3
  • 31
    • 85034127999 scopus 로고    scopus 로고
    • note
    • The racemization strongly depends on the reaction conditions and the catalyst used. Future experiments will attempt to determine the mechanism of the interconversion of the enantiomeric 3.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.