Progress toward the total synthesis of saudin: Development of a tandem Stille-oxa-electrocyclization reaction

Uttam K. Tambar, Taichi Kano, Brian M. Stoltz

Research output: Contribution to journalArticle

25 Scopus citations

Abstract

(Chemical Equation Presented) A diastereoselective tandem Stille-oxa-electrocyclization reaction provides access to the core of the diterpenoid natural product saudin. Additionally, this new reaction sequence was extended to the convergent preparation of related polycyclic pyran systems.

Original languageEnglish (US)
Pages (from-to)2413-2416
Number of pages4
JournalOrganic Letters
Volume7
Issue number12
DOIs
StatePublished - Jun 9 2005

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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