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Volumn 13, Issue 6, 2002, Pages 667-670

A new and efficient chemoenzymatic access to both enantiomers of 4-hydroxycyclopent-2-en-1-one

Author keywords

[No Author keywords available]

Indexed keywords

3 METHOXYCYCLOPENT 2 EN 1 ONE; 4 HYDROXYCYCLOPENT 2 EN 1 ONE; 5 ACETOXY 3 METHOXYCYCLOPENT 2 EN 1 ONE; 5 HYDROXY 3 METHOXYCYCLOPENT 2 EN 1 ONE; ACETIC ACID DERIVATIVE; KETONE DERIVATIVE; MANGANESE ACETATE; UNCLASSIFIED DRUG;

EID: 0037134290     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00168-4     Document Type: Article
Times cited : (19)

References (33)
  • 25
    • 0008890967 scopus 로고    scopus 로고
    • For high yield acetoxylation, manganese(III) acetate must be dried over phosphorus pentaoxide under vacuum prior to use.
  • 26
    • 0008890467 scopus 로고    scopus 로고
    • note
  • 33
    • 0008953034 scopus 로고    scopus 로고
    • LAH reduction reaction must be highly stereoselective to give the S,S (R,R) diol prior to hydrolysis and elimination of one of the OH groups. This reduction step is still under investigation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.