Litcius/Paper detail

A Powerful Chiral Super Brønsted C–H Acid for Asymmetric Catalysis

Bingfei Peng, Jiguo Ma, Jianhua Guo, Yating Gong, Ronghao Wang, Yi Zhang, Jinlong Zeng, Wenwen Chen, Kuiling Ding, Baoguo Zhao

2022Journal of the American Chemical Society62 citationsDOI

Abstract

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.

Topics & Concepts

ChemistryBrønsted–Lowry acid–base theoryCatalysisEnolAllylic rearrangementProtonationAminationEnantioselective synthesisOrganic chemistrySilyl etherSulfonylOrganocatalysisMedicinal chemistrySilylationIonAlkylAsymmetric Synthesis and CatalysisAsymmetric Hydrogenation and CatalysisSynthetic Organic Chemistry Methods