4.7 Article

Enantioselective direct aminalization with primary carboxamides catalyzed by chiral ammonium 1,1′-binaphthyl-2,2′-disulfonates

Journal

CHEMICAL COMMUNICATIONS
Volume 48, Issue 41, Pages 4986-4988

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cc31530k

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Funding

  1. MEXT [21200033]
  2. Yazaki Memorial Foundation for Science and Technology
  3. Grants-in-Aid for Scientific Research [24105512, 21200033] Funding Source: KAKEN

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A highly effective catalytic enantioselective direct aminal synthesis was developed. Chiral ammonium 1,1'-binaphthyl-2,2'-disulfonates, which were prepared in situ from (R)-BINSA and achiral amines, promoted the enantioselective addition of primary amides to aromatic aldimines.

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