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Volumn , Issue 7, 2006, Pages 1051-1054

Stereoselective synthesis of (+)-paeonilide and confirmation of its absolute configuration

Author keywords

(+) paeonilide; Absolute configuration; Carvone; Diastereoselective synthesis; Monoterpenoid

Indexed keywords

PAENILIDE; TERPENOID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33646756888     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-939698     Document Type: Article
Times cited : (9)

References (18)
  • 8
    • 0034838602 scopus 로고    scopus 로고
    • (b) For a high-yielding procedure leading to compound 6, see: Engel, W. J. Agric. Food Chem. 2001, 49, 4069.
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 4069
    • Engel, W.1
  • 12
    • 33646799059 scopus 로고    scopus 로고
    • note
    • In the synthetic work published in ref. 3, discriminating between the two primary hydroxyl groups was achieved by an enzymatic acetylation towards substrate 3 and diastereoisomeric monoacetate of diol 3 was obtained with a ratio of 13: 1. In our case, bromoetherification of diol 3 led to only desired diastereisomer 15.
  • 17
    • 33646773865 scopus 로고    scopus 로고
    • note
    • Natural paeonilide was provided by professor J. K. Liu. The optical rotation of synthetic paeonilide compared well to the value of authentic sample.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.