期刊
ORGANIC LETTERS
卷 22, 期 6, 页码 2240-2245出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.0c00442
关键词
-
资金
- Universite de Lyon [ANR-16_IDEX-0005]
- French Ministry of Higher Education and Research
A photoredox Ni-catalyzed cross-coupling of N-acylimides with unactivated alkyl bromides has been developed that enables efficient access to a variety of functionalized alkyl ketones, including unsymmetrical dialkyl ketones, under very mild and operationally practical conditions. The reaction that operates without the need for any preformed carbon nucleophile proceeds via the combination of two different bond activation processes, i.e. Ni-catalyzed imide activation via C(acyl)-N bond cleavage and (TMS)3Si radical-mediated alkyl halide activation via halogen-atom abstraction.
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