메뉴 건너뛰기




Volumn , Issue 3, 2006, Pages 403-406

Enantioconvergent access to the enantiomerically pure building blocks (+)-or (-)-4-hydroxy-3-methyl-2-cyclohexenone using a chemoenzymatic process

Author keywords

Biocatalysis; Chiral building blocks; Enantioconvergence; Kinetic Resolution; Stereoinversion

Indexed keywords

4 HYDROXY 3 METHYL 2 CYCLOHEXENONE; ACETIC ACID; ALCOHOL; KETONE DERIVATIVE; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

EID: 33344466637     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926258     Document Type: Article
Times cited : (8)

References (56)
  • 11
    • 0003548906 scopus 로고    scopus 로고
    • Koskinen, A. M. P.; Klibanov, A. M., Eds.; Blackie Academic and Professional: Glasgow
    • Recent books: (a) Enzymatic Reaction in Organic Media; Koskinen, A. M. P.; Klibanov, A. M., Eds.; Blackie Academic and Professional: Glasgow, 1996.
    • (1996) Enzymatic Reaction in Organic Media
  • 13
    • 0003993814 scopus 로고    scopus 로고
    • Patel, R. N., Ed.; Marcel Dekker, Inc.: New York
    • (c) Stereoselective Biocatalysis; Patel, R. N., Ed.; Marcel Dekker, Inc.: New York, 2000.
    • (2000) Stereoselective Biocatalysis
  • 49
    • 33344467014 scopus 로고    scopus 로고
    • note
    • 4: C, 58.05; H, 7.58. Found: C, 57.89; H, 7.60.
  • 55
    • 33344474695 scopus 로고    scopus 로고
    • note
    • CAL-B and RML lipases also showed high enantio-selectivity, but with a slightly lower ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.