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Catalyst Controlled Regiodivergent Arylboration of Dienes.


ABSTRACT: A method for the regiodivergent arylboration of dienes is presented. These reactions allow for the formation of a diverse range of synthetically versatile products from simple precursors. Through mechanistic studies, these reactions likely operate by initial addition of a Cu-Bpin complex across the diene followed by Pd-catalyzed cross coupling with an aryl halide or pseudohalide.

SUBMITTER: Sardini SR 

PROVIDER: S-EPMC5618444 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature

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Catalyst Controlled Regiodivergent Arylboration of Dienes.

Sardini Stephen R SR   Brown M Kevin MK  

Journal of the American Chemical Society 20170712 29


A method for the regiodivergent arylboration of dienes is presented. These reactions allow for the formation of a diverse range of synthetically versatile products from simple precursors. Through mechanistic studies, these reactions likely operate by initial addition of a Cu-Bpin complex across the diene followed by Pd-catalyzed cross coupling with an aryl halide or pseudohalide. ...[more]

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