电泳剂
芳基
化学
亲电胺化
催化作用
组合化学
烷基化
钯
酰化
胺化
有机化学
烷基
作者
Xiaotian Qi,Jian-Chun Wang,Zhe Dong,Guangbin Dong,Peng Liu
出处
期刊:Chem
[Elsevier]
日期:2020-10-01
卷期号:6 (10): 2810-2825
被引量:22
标识
DOI:10.1016/j.chempr.2020.09.004
摘要
A mechanistically guided approach is developed to predict electrophile compatibility in the palladium/norbornene (Pd/NBE) cooperative catalysis for the ipso and ortho difunctionalization of aryl halides. A key challenge in these reactions is to identify orthogonal electrophile and aryl halide starting materials that react selectively with different transition-metal complexes in separate oxidative addition events in the catalytic cycle. We performed detailed experimental and computational mechanistic studies to identify the catalytically active Pd(II) intermediate and the substrate-dependent mechanisms in reactions with various types of carbon and nitrogen electrophiles. We introduced the concept of electrophile compatibility score (ECS) to rationally select electrophiles based on the orthogonal reactivity of electrophile and aryl halide toward the Pd(0) and Pd(II) complexes. This approach was applied to predict the electrophile compatibility in the Pd/NBE cooperative catalysis with a variety of electrophilic coupling partners used in alkylation, arylation, amination, and acylation reactions.
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