Chemoselective Catalytic Dehydrogenative Cross-Coupling of 2‑Acylimidazoles: Mechanistic Investigations and Synthetic Scope
journal contributionposted on 30.07.2018, 00:00 by Tsukushi Tanaka, Kayoko Hashiguchi, Takafumi Tanaka, Ryo Yazaki, Takashi Ohshima
Chemoselective iron-catalyzed dehydrogenative cross-coupling using 2-acylimidazoles is described. The addition of a phosphine oxide ligand substantially facilitated the generation of tert-butoxy radicals from di-tert-butyl peroxide, allowing for efficient benzylic C–H bond cleavage under mild conditions. Extensive mechanistic studies revealed that the enolization of 2-acylimidazole proceeded through dual iron catalyst activation, followed by subsequent chemoselective cross-coupling with a benzyl radical over an undesired benzyl radical-derived homocoupling dimer that inevitably formed in earlier reported conditions. A variety of alkylarenes, aliphatic alkane, and functionalized 2-acylimidazoles were applicable, demonstrating the synthetic utility of the present catalysis. Contiguous all-carbon quaternary carbons were constructed through dehydrogenative cross-coupling. The catalytic chemoselective activation of 2-acylimidazole over bidentate coordinative and much more acidic malonate diester was particular noteworthy. Catalytic oxidative cross-enolate coupling of two distinct carboxylic acid equivalents was also achieved using acetonitrile as a coupling partner.
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Catalytic oxidative cross-enolateundesired benzyl radical-derived homocoupling dimertertContiguous all-carbon quaternary carbonsacidic malonate diestercarboxylic acid equivalentsfunctionalized 2- acylimidazolesChemoselective Catalytic Dehydrogenative Cross-Couplingphosphine oxide ligandchemoselective2- acylimidazoleSynthetic Scope Chemoselective iron-catalyzed dehydrogenative cross-couplingiron catalyst activation