4.7 Article

Asymmetric Strecker reaction of ketoimines catalyzed by a novel chiral bifunctional N,N′-dioxide

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 348, Issue 18, Pages 2579-2584

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.200600238

Keywords

asymmetric catalysis; ketoimines; organocatalyst; Strecker reaction

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A novel bifunctional N,N'-dioxide derived from L-prolinamide was employed to catalyze the enantioselective Strecker reaction of a range of N-tosyl ketoimines, and an effective additive was used to improve the reactivity (up to 99% yield) as well as the enantioselectivity (up to 91% ee). In addition, a rational transition state was proposed to elucidate the origin of chiral induction in which an S-adduct was produced.

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