Total synthesis of (-)-chokol A by an asymmetric domino Michael addition-Dieckmann cyclization

Synlett

Volumn , Issue 14, 2006, Pages 2223-2226

  Groth, Ulrich ^a   Kesenheimer, Christian ^a   Kreye, Paul ^a  

^a UNIVERSITY OF KONSTANZ   (Germany)

Author keywords

Antifungal agents; Asymmetric synthesis; Michael addition; Tandem reaction; Total synthesis

Indexed keywords

ANTIFUNGAL AGENT; BROMINE DERIVATIVE; CHOKOL A; ESTER DERIVATIVE; NATURAL PRODUCT; SESQUITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ASYMMETRIC SYNTHESIS; BENZYLATION; CARBONYLATION; CYCLIZATION; CYCLOPROPANATION; DIASTEREOISOMER; DIECKMANN REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; METHYLATION; MICHAEL ADDITION;

EID: 33748677051     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-949653     Document Type: Article

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