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Volumn , Issue 33, 2010, Pages 6354-6358

Asymmetric synthesis of O-protected acyloins using enoate reductases: Stereochemical control through protecting group modification

Author keywords

Asymmetric synthesis; Biocatalysis; Enones; Enzymes; Reduction

Indexed keywords


EID: 78649282252     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201001042     Document Type: Article
Times cited : (39)

References (42)
  • 10
    • 78649251679 scopus 로고    scopus 로고
    • For recent studies, see
    • For recent studies, see
  • 17
    • 78649310955 scopus 로고    scopus 로고
    • For a historical study and reviews, see
    • For a historical study and reviews, see
  • 23
    • 37049072996 scopus 로고
    • The bioreduction of diethyl oxaloacetate (which is in equilibrium with its enol form) by using baker's yeast proceeded through the carbonyl reductases acting on the keto form of the substrate.
    • The bioreduction of diethyl oxaloacetate (which is in equilibrium with its enol form) by using baker's yeast proceeded through the carbonyl reductases acting on the keto form of the substrate:, E. Santaniello, P. Ferraboschi, P. Grisenti, F. Aragozzini, E. Maconi, J. Chem. Soc. Perkin Trans. 1 1991, 601-605.
    • (1991) J. Chem. Soc. Perkin Trans. 1 , pp. 601-605
    • Santaniello, E.1    Ferraboschi, P.2    Grisenti, P.3    Aragozzini, F.4    MacOni, E.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.