Catalytic activation of nucleophile precursors with metal acetates in alcohol media and applications to enantioselective Michael addition reactions

Fumiyasu Ono, Masayuki Hasegawa, Shuji Kanemasa, Junji Tanaka

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Nickel(II) acetate tetrahydrate works as catalyst to activate nucleophile precursors in Michael addition reactions. Use of alcohol media is essential for the high catalytic activation of nucleophile precursors. Catalytic enantioselective reactions using a chiral nickel(II) acetate tetrahydrate between dimedone and α,β-unsaturated amide acceptors provide a useful synthetic access to enantiomers of enol lactones through the carbon-carbon bond formation.

Original languageEnglish
Pages (from-to)5105-5107
Number of pages3
JournalTetrahedron Letters
Volume49
Issue number34
DOIs
Publication statusPublished - Aug 18 2008

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All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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