Logo image
Home Academic units
Sign in
Catalytic Asymmetric Synthesis of Trifluoromethylated [gamma]-Amino Acids through the Umpolung Addition of Trifluoromethyl Imines to Carboxylic Acid Derivatives
Journal article   Peer reviewed

Catalytic Asymmetric Synthesis of Trifluoromethylated [gamma]-Amino Acids through the Umpolung Addition of Trifluoromethyl Imines to Carboxylic Acid Derivatives

Bin Hu and Li Deng
Angewandte Chemie, Vol.57(8), pp.2233-2237
02/19/2018

Abstract

Schiff bases Synthesis Enantiomers Organic compounds Cancer Chemotherapy Amino Acids
Novel cinchona alkaloid derived chiral phase-transfer catalysts enabled the highly chemo-, regio-, diastereo-, and enantioselective umpolung addition of trifluoromethyl imines to α,β-unsaturated N-acyl pyrroles. With a catalyst loading ranging from 0.2 to 5.0 mol %, this new catalytic asymmetric transformation provides facile and high-yielding access to highly enantiomerically enriched chiral trifluoromethylated γ-amino acids and γ-lactams.

UN Sustainable Development Goals (SDGs)

This output has contributed to the advancement of the following goals:

#6 Clean Water and Sanitation

Metrics

34 Record Views

Details