Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Department of Chemistry, Zhejiang Normal University , 688 Yingbin Road, Jinhua 321004, China.
Org Lett. 2018 Mar 2;20(5):1435-1438. doi: 10.1021/acs.orglett.8b00221. Epub 2018 Feb 13.
A novel nickel-catalyzed remote arylation of alkenyl aldehydes triggered by radical alkylation with tertiary α-carbonyl alkyl bromides is described, thus producing a quaternary carbon center containing ketones in promising yields with broad functional group compatibility. Preliminary mechanistic studies suggest that the combination of a 1,n-HAT (n = 5 or 6) from alkyl radicals to aldehyde C-H bonds with nickel catalysis may account for the realization of this reaction.
本文描述了一种新型的镍催化远程烯基醛的芳基化反应,该反应是通过叔α-羰基溴代烷烃的自由基烷基化引发的,从而以优异的收率和广泛的官能团兼容性得到了含有季碳中心的酮。初步的机理研究表明,从烷基自由基到醛 C-H 键的 1,n-HAT(n = 5 或 6)与镍催化的结合可能是实现该反应的原因。