메뉴 건너뛰기




Volumn 20, Issue , 1999, Pages 29-68

Designed syntheses of chiral compounds mediated by biocatalysts: Production of a desired stereoisomer

Author keywords

Alcohol; Asymmetric synthesis; Biocatalysis; Chirality; Chirality pump; Diastereoselectivity; Diketone; Enantioselectivity; Enzyme; Keto ester

Indexed keywords


EID: 0033424282     PISSN: 09156151     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (5)

References (32)
  • 1
    • 0003467672 scopus 로고
    • McGraw-Hill Book, New York
    • Any reaction in which only one of a set of stereoisomers is formed exclusively or predominantly is called stereoselective. In a stereospecific reaction, a given isomer leads to one product, while another steroisomer leads to the opposite product. Therefore, all enzymatic reactions with their natural substrates are stereoselective, but this is not true when an artificial substrate is fed to a microorganism: J. March: Advanced Organic Chemistry (McGraw-Hill Book, New York, 1968) p. 101.
    • (1968) Advanced Organic Chemistry , pp. 101
    • March, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.