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Iridium-catalyzed enantioselective addition of an <i>N</i>-methyl C–H bond to α-trifluoromethylstyrenes <i>via</i> C–H activation

Daisuke Yamauchi, Ikumi Nakamura, Takahiro Nishimura

2021Chemical Communications20 citationsDOI

Abstract

C-H activation to give chiral γ-branched amine derivatives having a trifluoromethyl-substituted stereocenter. It was found that a bulky and electron-withdrawing group at the 3-position of 2-(methylamino)pyridines was necessary for the present C-H addition reaction catalyzed by a cationic iridium/chiral bisphosphine complex.

Topics & Concepts

IridiumEnantioselective synthesisChemistryCationic polymerizationStereocenterCatalysisPyridineTrifluoromethylMedicinal chemistryAmine gas treatingStereochemistryOrganic chemistryAlkylFluorine in Organic ChemistryCatalytic C–H Functionalization MethodsCyclopropane Reaction Mechanisms
Iridium-catalyzed enantioselective addition of an <i>N</i>-methyl C–H bond to α-trifluoromethylstyrenes <i>via</i> C–H activation | Litcius