4.7 Article

Chiral iminophosphorane catalyzed asymmetric sulfenylation of 4-substituted pyrazolones

Journal

CHEMICAL COMMUNICATIONS
Volume 55, Issue 3, Pages 397-400

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8cc09049a

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Funding

  1. National Natural Science Foundation of China [NSFC 21472213]
  2. National Key Research and Development Program [2016YFA0200302]
  3. Croucher Foundation (Hong Kong)

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An excellent level of enantioselectivity in asymmetric sulfenylation of 4-substituted pyrazolones was achieved with chiral iminophosphorane as the organocatalyst under continuum solvation conditions (up to 99% ee). Importantly, this catalytic process features high efficiency with excellent enantioselectivities, easy separation of products, low catalytic loadings and scale-up to grams without loss of enantioselectivity.

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