Stereoselective synthesis of cyercene A and the placidenes

Guangxin Liang, Aubry K. Miller, Dirk Trauner

Research output: Contribution to journalArticle

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

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Pyrones
Biological Products
Polyenes
synthesis
products
cyercene A
stannane

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Stereoselective synthesis of cyercene A and the placidenes. / Liang, Guangxin; Miller, Aubry K.; Trauner, Dirk.

In: Organic Letters, Vol. 7, No. 5, 03.03.2005, p. 819-821.

Research output: Contribution to journalArticle

Liang, G, Miller, AK & Trauner, D 2005, 'Stereoselective synthesis of cyercene A and the placidenes', Organic Letters, vol. 7, no. 5, pp. 819-821. https://doi.org/10.1021/ol047542w
Liang, Guangxin ; Miller, Aubry K. ; Trauner, Dirk. / Stereoselective synthesis of cyercene A and the placidenes. In: Organic Letters. 2005 ; Vol. 7, No. 5. pp. 819-821.
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