马尔科夫尼科夫法则
区域选择性
化学
催化作用
磷化矿
原子经济
反应条件
组合化学
有机化学
协议(科学)
激进的
纳米技术
药物化学
立体选择性
作者
Yifan Li,Hong‐Chen Wang,Bing Han
标识
DOI:10.1038/s41467-026-72870-2
摘要
Abstract The phosphorylation of alkenes offers a diverse handle for obtaining organophosphoryls, but its regioselectivity still faces challenges, especially the radical Markovnikov hydrophosphorylation of alkenes. Herein, we develop a radical Markovnikov hydrophosphorylation of unactivated alkenes by a sequential reaction of (bis)homoallylic alcohols, Ph 2 PCl, and water under visible light-driven triple catalysis. The protocol initiates from a Co-H species-mediated metal-hydride atom transfer, followed by a water-mediated radical-polar crossover phosphinite rearrangement. This reaction features mild reaction conditions, excellent regio-/stereoselectivity, and good natural products compatibility. The successful radical deuterophosphonation of olefins by using D 2 O to replace H 2 O further demonstrates the synthetic value of the protocol. This protocol not only broadens the mode of phosphinite rearrangement, but also provides a successful example for the radical activation of water and its three-atom splitting and utilization in organic conversion.
科研通智能强力驱动
Strongly Powered by AbleSci AI