Enantioconvergent route to a functionalized quinane system

T. Yoshimitsu, Y. Ohshiba, K. Ogasawara

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)

Abstract

Enantioconvergent route to both enantiomers of a functionalized quinane, methyl 6-oxo-cis-bicyclo[3.3.0]oct-7-ene-3-endo-carboxylate, has been developed by employing lipase-mediated resolution and Wharton rearrangement.

Original languageEnglish
Pages (from-to)1029-1031
Number of pages3
JournalSynthesis
Issue number10
DOIs
Publication statusPublished - Jan 1 1994
Externally publishedYes

Keywords

  • Wharton reaction
  • enantioconvergent synthesis
  • lipase-mediated kinetic acylation
  • lipase-mediated resolution
  • quinane

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

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