选择性
化学
配体(生物化学)
镍
催化作用
组合化学
磷化氢
基质(水族馆)
联苯
有机化学
生物化学
海洋学
地质学
受体
作者
Shan Jiang,Tianze Zhang,Xiaoyuan Luo,Shou‐Cheng Dong,Jin-Tao Ma,Li‐Jun Xiao
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-04-03
卷期号:64 (24): e202504494-e202504494
被引量:15
标识
DOI:10.1002/anie.202504494
摘要
The regiodivergent carbosilylation of 1,3-dienes presents a formidable challenge due to inherently complex selectivity control over multiple potential reaction pathways. Here, we report a ligand-controlled, regiodivergent carbosilylation of 1,3-dienes with aldehydes and silylboranes, achieving unprecedented site-selectivity using nickel catalysts with distinct phosphine ligands. The use of triethylphosphine promotes 4,3-addition selectivity, while employing (2-biphenyl)dicyclohexylphosphine facilitates 4,1-addition selectivity. This method displays excellent regio- and diastereoselectivity, as well as a broad substrate scope and substantial functional group tolerance. Mechanistic studies indicate that the ligand choice is crucial for directing the reaction pathway and stabilizing π-allyl-nickel intermediates. Our protocol provides a practical and efficient approach to synthesizing valuable functionalized allylsilanes, which are important in various synthetic applications.
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