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Volumn 20, Issue 22, 2009, Pages 2622-2628

Chemo-enzymatic asymmetric total synthesis of stagonolide-C

Author keywords

[No Author keywords available]

Indexed keywords

LACTONE DERIVATIVE; STAGONOLIDE C; UNCLASSIFIED DRUG;

EID: 72049102361     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.10.007     Document Type: Article
Times cited : (51)

References (30)
  • 18
    • 72049115982 scopus 로고    scopus 로고
    • The enantioselectivity was determined by Chiral-HPLC (CHIRALPAK OJ-H, 254 nm) by deprotecting the acetate group and converting the free alcohol group to its benzoate ester.
    • The enantioselectivity was determined by Chiral-HPLC (CHIRALPAK OJ-H, 254 nm) by deprotecting the acetate group and converting the free alcohol group to its benzoate ester.
  • 22
    • 72049132030 scopus 로고    scopus 로고
    • The enantioselectivity of this step was determined by measuring the specific rotation value of 1,3-butanediol (obtained from 10 after successive deprotection of acetate and PMB group) and comparing with that of authentic sample.
    • The enantioselectivity of this step was determined by measuring the specific rotation value of 1,3-butanediol (obtained from 10 after successive deprotection of acetate and PMB group) and comparing with that of authentic sample.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.