A chemoenzymatic and enantioselective total synthesis of the resorcylic acid lactone L-783,290, the trans-isomer of L-783,277

Tetrahedron Letters

Volumn 51, Issue 7, 2010, Pages 1044-1047

  Lin, Andrew ^a   Willis, Anthony C ^a   Banwell, Martin G ^a  

^a AUSTRALIAN NATIONAL UNIVERSITY   (Australia)

Author keywords

Chemoenzymatic; Heck reaction; Resorcylic acid lactones; Ring closing metathesis; Synthesis

Indexed keywords

ALPHA RESORCYLIC ACID; CHLOROBENZENE; L 783277; L 783290; LACTONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; ENANTIOSELECTIVITY; TRANS ISOMER;

EID: 73649140608     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.12.067     Document Type: Article

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