Enantioselective organocatalytic double Michael addition reactions

  • Hao Li
  • , Liansuo Zu
  • , Hexin Xie
  • , Jian Wang
  • , Wei Jiang
  • , Wei Wang

Research output: Contribution to journalArticlepeer-review

160 Scopus citations

Abstract

A novel organocatalytic, enantioselective domino double Michael addition reaction of α,β-unsaturated aldehydes with ethyl 4-mercapto-2- butenoate has been developed. The process is promoted by chiral diphenylprolinol TMS ether to give chiral tetrahydrothiophenes in high to excellent levels of enantioselectivities.

Original languageEnglish (US)
Pages (from-to)1833-1835
Number of pages3
JournalOrganic Letters
Volume9
Issue number9
DOIs
StatePublished - Apr 26 2007
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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