Synthesis of 1,1-diboronate esters by cobalt-catalyzed sequential hydroboration of terminal alkynes

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Abstract

A cobalt complex of iminopyridine-oxazoline catalyzes sequential hydroboration of alkyl and aryl alkynes with pinacolborane to form 1,1-diboronate esters. The reactions proceed under mild conditions with high yields, high regioselectivity, and wide functional group tolerance. The synthetic utility of 1,1-di(boronates) is demonstrated by chemoselective monoarylation and stepwise diarylation through palladium-catalyzed Suzuki-Miyaura coupling reactions.

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Zuo, Z., & Huang, Z. (2016). Synthesis of 1,1-diboronate esters by cobalt-catalyzed sequential hydroboration of terminal alkynes. Organic Chemistry Frontiers, 3(4), 434–438. https://doi.org/10.1039/c5qo00426h

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