催化作用
镍
芳基
催化循环
磷化氢
配体(生物化学)
化学
组合化学
对映选择合成
光化学
有机化学
烷基
生物化学
受体
作者
Ramon Arora,Mark Lautens
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-01-22
卷期号:14 (3): 1970-1975
被引量:19
标识
DOI:10.1021/acscatal.3c05994
摘要
A nickel/blue light-catalyzed carbohalogenation reaction is reported. A nickel catalyst and an inexpensive phosphine ligand promote the reaction of aryl iodides and aryl bromides with π systems to enable the construction of a library of halogenated heterocyclic scaffolds. Mechanistic studies provide insight regarding fundamental steps of the catalytic cycle, including the reversible C–X bond formation via deuterium labeling and EPR experiments, while preliminary enantioselective results suggest a two-electron migratory insertion.
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