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A Powerful Chiral Super Brønsted C-H Acid for Asymmetric Catalysis.

Bingfei PengJiguo MaJianhua GuoYating GongRonghao WangYi ZhangJinlong ZengWen-Wen ChenKui-Ling DingBaoguo Zhao
Published in: Journal of the American Chemical Society (2022)
A new type of chiral super Brønsted C-H acids, BINOL-derived phosphoryl bis((trifluoromethyl)sulfonyl) methanes (BPTMs), were developed. As compared to widely utilized BINOL-derived chiral phosphoric acids (BPAs) and N -triflyl phosphoramides (NTPAs), BPTMs displayed much higher Brønsted acidity, resulting in dramatically improved activity and excellent enantioselectivity as demonstrated in catalytic asymmetric Mukaiyama-Mannich reaction, allylic amination, three-component coupling of allyltrimethylsilane with 9-fluorenylmethyl carbamate and aldehydes, and protonation of silyl enol ether. These new strong Brønsted C-H acids have provided a platform for expanding the chemistry of asymmetric Brønsted acid catalysis.
Keyphrases
  • ionic liquid
  • capillary electrophoresis
  • solid state
  • mass spectrometry
  • visible light
  • crystal structure
  • drug discovery