Total synthesis of amphidinolide T3 using ring-closing metathesis and asymmetric dihydroxylation strategy

Synlett

Volumn , Issue 7, 2011, Pages 895-898

  Wu, Dongdong ^a   Li, Huoming ^a,b   Jin, Jian ^b   Wu, Jinlong ^a   Dai, Wei Min ^a,b  

^a ZHEJIANG UNIVERSITY   (China)

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

Author keywords

metathesis; amphidinolide T3; dihydroxylation; macrocycles; total synthesis

Indexed keywords

AMPHIDINOLIDE T3; MACROLIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; DESILYLATION; DIHYDROXYLATION; DRUG STRUCTURE; EPIMERIZATION; ESTERIFICATION; HUMAN; HYDROGENATION; LACTONIZATION; NONHUMAN; OXIDATION; RING CLOSING METATHESIS; SILYLATION; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 79954624824     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0030-1259706     Document Type: Article

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