Synthesis of two diastereomers of iriomoteolide-1a via a tunable four-module coupling approach using ring-closing metathesis as the key step

Synlett

Volumn , Issue 12, 2011, Pages 1774-1778

  Liu, Yuanxin ^a   Feng, Gaofeng ^b   Wang, Jian ^a   Wu, Jinlong ^a   Dai, Wei Min ^a,b  

^a ZHEJIANG UNIVERSITY   (China)

^b HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Hong Kong)

Author keywords

iriomoteolide; macrolide; modular synthesis; ring closing metathesis; stereoisomers

Indexed keywords

ALKADIENE; CYCLOALKENE; IRIOMOTEOLIDE 1A; IRIOMOTEOLIDE 1B; MACROLIDE; METAL DERIVATIVE; UNCLASSIFIED DRUG;

ALDOL REACTION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CHIRALITY; CROSS COUPLING REACTION; DIASTEREOISOMER; RING CLOSING METATHESIS;

EID: 79960251804     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1260822     Document Type: Article

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