4.7 Article

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

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ORGANIC CHEMISTRY FRONTIERS
卷 3, 期 4, 页码 434-438

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c5qo00426h

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资金

  1. National Basic Research Program of China [2015CB856600]
  2. National Natural Science Foundation of China [21422209, 21272255, 21432011, 21421091]
  3. CAS/SAFEA International Partnership Program for Creative Research Teams

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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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