Chemoselective <i>α</i>‐Alkylation of Nitriles with Primary Alcohols by Manganese(I)‐Catalysis
Krishanu Bera, Arup Mukherjee
Abstract
A sustainable and easy-to-use protocol for the alkylation of aryl nitriles with the earth-abundant manganese(I) catalyst is presented. The alkylation reaction employs readily available nitriles and naturally abundant alcohols as the coupling partners. The reaction proceeds chemoselectively and encompasses a broad substrate scope with good to excellent yields. The catalytic reaction yields selectively α-branched nitriles and water as the sole byproduct. Experimental studies were executed to understand the mechanism of the catalytic reaction.
Topics & Concepts
AlkylationCatalysisManganeseChemistryPrimary (astronomy)ArylOrganic chemistrySubstrate (aquarium)Combinatorial chemistryScope (computer science)AlkylGeologyPhysicsOceanographyAstronomyProgramming languageComputer scienceAsymmetric Hydrogenation and CatalysisChemical Synthesis and ReactionsCatalytic C–H Functionalization Methods