Stereoselective synthesis of cyercene A and the placidenes

Guangxin Liang, Aubry K. Miller, Dirk Trauner

Research output: Contribution to journalArticlepeer-review

Abstract

(Chemical Equation Presented) Members of a family of α-methoxy-y- pyrone-containing polypropionate natural products have been stereoselectively synthesized. Two key iodovinyl pyrone building blocks were coupled to appropriately selected vinyl stannanes to assemble the highly substituted polyene side chains of the natural products.

Original languageEnglish (US)
Pages (from-to)819-821
Number of pages3
JournalOrganic Letters
Volume7
Issue number5
DOIs
StatePublished - Mar 3 2005

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Stereoselective synthesis of cyercene A and the placidenes'. Together they form a unique fingerprint.

Cite this