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Volumn 343, Issue 6-7, 2001, Pages 646-654

Kinetic Resolution of (±)-1-Phenylbutan-1-ol by Means of CALB-Catalyzed Aminolyses: A Study on the Role of the Amine in the Alcohol Resolution

Author keywords

Alcohols; Amines; Chiral resolution; Enantioselectivity; Enzyme catalysis

Indexed keywords


EID: 0347036828     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/1615-4169(200108)343:6/7<646::aid-adsc646>3.0.co;2-a     Document Type: Article
Times cited : (17)

References (36)
  • 14
    • 0034608087 scopus 로고    scopus 로고
    • F. Theil, Tetrahedron 2000, 56, 2905-2919.
    • (2000) Tetrahedron , vol.56 , pp. 2905-2919
    • Theil, F.1
  • 28
    • 0348029655 scopus 로고    scopus 로고
    • Two different binding modes can be assumed for the achiral benzylamine (4) analogous to those ones adopted by the R- and S-enantiomers of the chiral amines 3 and 5-7. They arise from considering the phenyl ring as the large-sized substituent and one of the two hydrogen atoms as the medium-sized substituent
    • Two different binding modes can be assumed for the achiral benzylamine (4) analogous to those ones adopted by the R- and S-enantiomers of the chiral amines 3 and 5-7. They arise from considering the phenyl ring as the large-sized substituent and one of the two hydrogen atoms as the medium-sized substituent.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.