Deoxygenative hydroboration of carboxamides: A versatile and selective synthetic approach to amines
Khalimon A.Y.
21 December 2021Royal Society of Chemistry
Dalton Transactions
2021#50Issue 4717455 - 17466 pp.
Deoxygenative reduction of amides is considered as an attractive method for preparation of synthetically valuable amines. However, the low electrophilicity of the amide carbonyl group, high thermodynamic stability and kinetic inertness of the amides make their reduction a challenging task. Until recently, most efforts for catalytic deoxygenation of amides to amines were concentrated on hydrogenation and hydrosilylation approaches, which mainly employed precious metal catalysts and often required harsh reaction conditions and showed insufficient selectivities. Moreover, these reactions are mostly limited to secondary and tertiary amides, whereas direct reduction of primary amides to primary amines remained arduous. In contrast, deoxygenative hydroboration of amides, although it appeared less then a decade ago, has already proved advantageous in terms of the amide scope, reaction conditions and selectivity of transformations. This article provides an overview of the developments in hydroboration of amides, focusing on mechanistic aspects of these transformations and advantages of hydroboration compared to hydrogenation and hydrosilylation approaches.
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Department of Chemistry, School of Sciences and Humanities, Nazarbayev University, 53 Kabanbay Batyr Avenue, Nur-Sultan, 010000, Kazakhstan
Department of Chemistry
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