Diastereoselective epoxidation of camphor N-enoylpyrazolidinones

Chai Ling Fan, Gondi Sudershan Reddy, Kwunmin Chen

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Reaction of camphor N-enoylpyrazolidinones (1a-j) with various oxidants, in particular UHP/TFAA afford chiral epoxides with a wide range of stereoselectivities (up to > 90% de).

Original languageEnglish
Pages (from-to)1047-1051
Number of pages5
JournalJournal of the Chinese Chemical Society
Volume50
Issue number5
DOIs
Publication statusPublished - 2003 Jan 1

Keywords

  • Asymmetric
  • Camphor
  • Chiral auxiliary
  • Diastereoselectivity
  • Epoxide
  • Lewis acid
  • Mechanism
  • Stereoinduction

ASJC Scopus subject areas

  • Chemistry(all)

Fingerprint Dive into the research topics of 'Diastereoselective epoxidation of camphor N-enoylpyrazolidinones'. Together they form a unique fingerprint.

  • Cite this