articleAccounts of Chemical ResearchAug 13, 2002Closed access

N-tert -Butanesulfinyl Imines:  Versatile Intermediates for the Asymmetric Synthesis of Amines

University of California, Berkeley

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Abstract

N-tert-Butanesulfinyl aldimines 3 and ketimines 4 are exceedingly versatile intermediates for the asymmetric synthesis of amines. The N-tert-butanesulfinyl imines are prepared in high yields by condensing enantiomerically pure tert-butanesulfinamide 1, which is readily available in either configuration, with a wide range of aldehydes and ketones. The tert-butanesulfinyl group activates the imines for the addition of many different classes of nucleophiles, serves as a powerful chiral directing group, and after nucleophilic addition is readily cleaved by treatment of the product with acid. A wide range of highly enantioenriched amines, including alpha-branched and alpha,alpha-dibranched amines, alpha- and…

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Authors

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Topics & keywords

Keywords
  • Aldimine
  • Imine
  • Chemistry
  • Nucleophile
  • Enantioselective synthesis
  • Nucleophilic addition
  • Catalysis
  • Trifluoromethyl
UN Sustainable Development Goals
  • Clean water and sanitation
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