An enantioselective, modular, and general route to the cytochalasins: Synthesis of L-696,474 and cytochalasin B

Proceedings of the National Academy of Sciences of the United States of America

Volumn 101, Issue 33, 2004, Pages 12048-12053

  Haidle, Andrew M ^a   Myers, Andrew G ^a  

^a HARVARD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO COMPOUND; CYTOCHALASIN B; CYTOCHALASIN DERIVATIVE; ISOINDOLE DERIVATIVE; L 696474; LACTONE DERIVATIVE; MACROCYCLIC COMPOUND; NATURAL PRODUCT; PROTEINASE; PROTEINASE INHIBITOR;

ACTIN FILAMENT; ANGIOGENESIS; ARTICLE; DIELS ALDER REACTION; DRUG SYNTHESIS; ENANTIOSELECTIVITY; PRIORITY JOURNAL; REACTION ANALYSIS; STRUCTURE ACTIVITY RELATION;

CHEMISTRY, ORGANIC; CYTOCHALASIN B; CYTOCHALASINS; MOLECULAR STRUCTURE; STEREOISOMERISM;

BETULACEAE;

EID: 4344691847     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0402111101     Document Type: Article

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