The enantioselective cobalt(III)-catalyzed C−H alkylation was achieved through the design of a novel chiral acid. The cobalt(III)-catalyzed enantioselective C−H activation was characterized by high position-, regio- and enantio-control under exceedingly mild reaction conditions. Thereby, the robust cooperative cobalt(III) catalysis proved tolerant of valuable electrophilic functional groups, including hydroxyl, bromo, and iodo substituents. Mechanistic studies revealed a considerable additive effect on kinetics and on a negative non-linear-effect.

Enantioselective Cobalt(III)-Catalyzed C−H Activation Enabled by Chiral Carboxylic Acid Cooperation

Pesciaioli F.;
2018

Abstract

The enantioselective cobalt(III)-catalyzed C−H alkylation was achieved through the design of a novel chiral acid. The cobalt(III)-catalyzed enantioselective C−H activation was characterized by high position-, regio- and enantio-control under exceedingly mild reaction conditions. Thereby, the robust cooperative cobalt(III) catalysis proved tolerant of valuable electrophilic functional groups, including hydroxyl, bromo, and iodo substituents. Mechanistic studies revealed a considerable additive effect on kinetics and on a negative non-linear-effect.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/150181
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