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Total synthesis of (+)-crocacin C.
Feutrill, J T; Lilly, M J; Rizzacasa, M A.
Affiliation
  • Feutrill JT; School of Chemistry, The University of Melbourne, Victoria 3010, Australia.
Org Lett ; 2(21): 3365-7, 2000 Oct 19.
Article in En | MEDLINE | ID: mdl-11029212
The first asymmetric synthesis of (+)-crocacin C (3) is described which served to confirm the absolute configuration of this compound. The key step in the sequence was the stereoselective assembly of the (E,E)-diene amide side chain by a Stille cross-coupling between the stannane 5 and vinyl iodide 6.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Antifungal Agents Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2000 Document type: Article Affiliation country: Australia Country of publication: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Antifungal Agents Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2000 Document type: Article Affiliation country: Australia Country of publication: United States