Nickel-catalysed cross-electrophile coupling of aryl bromides and primary alkyl bromides

RSC Adv. 2022 Jan 26;12(6):3569-3572. doi: 10.1039/d2ra00010e. eCollection 2022 Jan 24.

Abstract

The structure of primary alkylated arenes plays an important role in the molecular action of drugs and natural products. The nickel/spiro-bidentate-pyox catalysed cross-electrophile coupling of aryl bromides and primary alkyl bromides was developed for the formation of the Csp2-Csp3 bond, which provided an efficient method for the synthesis of primary alkylated arenes. The reactions could tolerate functional groups such as ester, aldehyde, ketone, ether, benzyl, and imide.