4.7 Article

Ligand-metal cooperativity in quinonoid based nickel(ii) and cobalt(ii) complexes for catalytic hydrosilylative reduction of nitriles to amines: electron transfer and mechanistic insight

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Base-Catalyzed Hydrosilylation of Nitriles to Amines and Esters to Alcohols

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Summary: The study presents a base-catalyzed hydrosilylation of nitriles to amines and esters to silylated alcohols, showing successful reactions in the presence of basic functional groups but failure for acidic substrates. Carbonyl functional groups, such as aldehydes, ketones, esters and carbamides, are reduced to corresponding alcohols and amines. Ester reduction can be selective in the presence of nitriles, but selectivity decreases for ester/carboxamide and carboxamide/nitrile pairs. Competitive experiments determined the preference in functional group reactivity as ester > carboxamide > nitrile.

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