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Volumn 123, Issue 37, 2001, Pages 9033-9044
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A general strategy for the synthesis of cladiellin diterpenes: Enantioselective total syntheses of 6-acetoxycladiell-7(16),11-dien-3-ol (deacetoxyalcyonin acetate), cladiell-11-ene-3,6,7-triol, sclerophytin A, and the initially purported structure of sclerophytin A
a,b a a |
Author keywords
[No Author keywords available]
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Indexed keywords
PHOTOLYTIC DEFORMYLATION;
ALCOHOLS;
CONDENSATION;
HYDRIDES;
STEREOCHEMISTRY;
SYNTHESIS (CHEMICAL);
AROMATIC COMPOUNDS;
ALDEHYDE DERIVATIVE;
ALLYL ALCOHOL;
ALLYL COMPOUND;
BENZOFURAN DERIVATIVE;
CARBON;
CARVONE;
CLADIELL 11 ENE 3,6,7 TRIOL;
DEACETOXYALCYONIN ACETATE;
DITERPENE;
ETHER DERIVATIVE;
GLYCIDOL;
HYDROXYL GROUP;
SCLEROPHYTIN A;
UNCLASSIFIED DRUG;
ARTICLE;
CHEMICAL BINDING;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
EPOXIDATION;
ISOMERISM;
POLYMERIZATION;
REACTION ANALYSIS;
REDUCTION;
STEREOCHEMISTRY;
SYNTHESIS;
BRIDGED COMPOUNDS;
DITERPENES;
FURANS;
STEREOISOMERISM;
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EID: 0035913709
PISSN: 00027863
EISSN: None
Source Type: Journal
DOI: 10.1021/ja016351a Document Type: Article |
Times cited : (101)
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References (141)
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