Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba, 2608675, Japan.
Org Biomol Chem. 2019 May 15;17(19):4783-4788. doi: 10.1039/c9ob00637k.
An efficient synthesis of carbo- and heterocycles using C[double bond, length as m-dash]C, C[double bond, length as m-dash]O and C[double bond, length as m-dash]N bonds under cobalt catalysis is described. The substituents on olefins are key for controlling the regio- and chemoselectivity in the initial hydrogen atom transfer step and quaternary carbons are efficiently constructed under mild conditions. Cyclopropane cleavage and tandem cyclization give highly functionalized bicyclic skeletons in a single operation.
本文描述了钴催化下通过 C[双键,长度为破折号]C、C[双键,长度为破折号]O 和 C[双键,长度为破折号]N 键合成碳环和杂环化合物的有效方法。烯烃上的取代基是控制初始氢原子转移步骤区域和化学选择性的关键,在温和条件下可有效地构建季碳原子。环丙烷的开环和串联环化可以在一步反应中得到高度官能化的双环骨架。