化学
催化作用
分子间力
选择性
光化学
氢键
氢原子
有机化学
分子
烷基
作者
Laura K. G. Ackerman,Jesus I. Martinez Alvarado,Abigail G. Doyle
摘要
A method for direct cross coupling between unactivated C(sp3)-H bonds and chloroformates has been accomplished via nickel and photoredox catalysis. A diverse range of feedstock chemicals, such as (a)cyclic alkanes and toluenes, along with late-stage intermediates, undergo intermolecular C-C bond formation to afford esters under mild conditions using only 3 equiv of the C-H partner. Site selectivity is predictable according to bond strength and polarity trends that are consistent with the intermediacy of a chlorine radical as the hydrogen atom-abstracting species.
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