期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 142, 期 7, 页码 3532-3539出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.9b12490
关键词
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资金
- King Abdullah University of Science and Technology (KAUST)
- European Research Council under the European Union's Seventh Framework Programme (FP/2007-2013)/ERC Grant [617044]
Cross-coupling reactions for carbon-carbon and carbon-heteroatom bond formation are of great importance in modern chemical synthesis. In addition to classical cross-couplings involving preformed or preactivated coupling partners, more recently breakthroughs have been made in the selective, direct coupling of abundant aliphatic carbon-hydrogen bonds using hydrogen atom transfer reactions in which the bond-dissociation energy is the thermodynamic driving force. The more challenging carbon-carbon bond activation is still rather underdeveloped due to the bond inertness. Herein, we report a mild and general strategy for the activation of a diverse set of readily available cyclic alcohols for the remote and site-specific arylation of ketones via the combination of photoredox-mediated multisite concerted proton-electron transfer (MS-PCET) and nickel catalysis. The current cross-coupling proceeds with the generation of an alkoxy radical utilizing bond-dissociation free energy (BDFE) as the thermodynamic driving force. Subsequently, the resulting remote carbon-centered radicals formed by C-C cleavage merge with the nickel catalytic cycle to create the challenging C(sp(3))-C(sp(2)) bonds.
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