4.8 Article

Chiral Tetraaminophosphonium Carboxylate-Catalyzed Direct Mannich-Type Reaction

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 43, 页码 14088-+

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AMER CHEMICAL SOC
DOI: 10.1021/ja806311e

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  1. Kurata Memorial Hitachi Science and Technology Foundation
  2. Nagoya University
  3. MEXT, Japan

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The cooperative asymmetric catalysis of chiral tetraaminophosphonium carboxylate (P,S)-1-OCOR has been established, and its synthetic utility has been successfully demonstrated by application to the highly enantioselective direct Mannich-type reaction of azlactones with N-sulfonyl imines. The present study stimulates the cultivation of the potential of the chiral quaternary onium salt catalysis by the structural modification of organic anion.

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