Abstract

Copper-catalyzed borocarbonylation of terminal alkenes usually gives terminal boron substituted β-boryl carbonyl compounds. In this communication, a copper-catalyzed selectivity-reversed borocarbonylation has been described. In the presence of CuOAc/BuPAd2 catalytic system, a series of unactivated terminal alkenes were transformed into β-boryl ketones in moderate yields, with sterically hindered alkyl bromides as the electrophiles.

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