An efficient method for the synthesis of enol ethers and enecarbamates. Total syntheses of isoindolobenzazepine alkaloids, lennoxamine and chilenine

Haruhiko Fuwa, Makoto Sasaki

Research output: Contribution to journalArticlepeer-review

38 Citations (Scopus)

Abstract

An efficient method for the synthesis of enol ethers and enecarbamates has been developed based on catalytic hydrosilane reduction of α-phosphonoxy enol ethers and α-phosphonoxy enecarbamates. This method has been applied to the total syntheses of two isoindolobenzazepine alkaloids, lennoxamine and chilenine.

Original languageEnglish
Pages (from-to)1849-1853
Number of pages5
JournalOrganic and Biomolecular Chemistry
Volume5
Issue number12
DOIs
Publication statusPublished - 2007 Jun 14

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'An efficient method for the synthesis of enol ethers and enecarbamates. Total syntheses of isoindolobenzazepine alkaloids, lennoxamine and chilenine'. Together they form a unique fingerprint.

Cite this