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Diastereoselectivity in Michael additions to a pyrrolidinyl enone

  • Chulalongkorn University
  • Chulabhorn Research Institute

Research output: Contribution to journal › Article › peer-review

6 Citations (Scopus)

Abstract

Michael additions of stabilized carabanions to an α-pyrrolidinylenone are highly diastereoselective. Epoxidation is similarly selective.

Original languageEnglish
Pages (from-to)1307-1309
Number of pages3
JournalSynlett
Issue number8
DOIs
Publication statusPublished - 1999

Keywords

  • Diastereoselectivity
  • Epoxidation
  • Michael addition

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