Enantioconvergent route to a functionalized quinane system

T. Yoshimitsu, Y. Ohshiba, K. Ogasawara

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


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
Issue number10
Publication statusPublished - Jan 1 1994
Externally publishedYes


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

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Enantioconvergent route to a functionalized quinane system'. Together they form a unique fingerprint.

Cite this