化学
卤化物
烷基
催化作用
镍
光催化
氢原子
光化学
过渡金属
药物化学
有机化学
作者
Ramadevi Pilli,Keerthika Selvam,Bala S. S. Balamurugan,Vidya Jose,Ramesh Rasappan
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-04-09
卷期号:26 (15): 2993-2998
被引量:11
标识
DOI:10.1021/acs.orglett.4c00567
摘要
Functionalization of C(sp3)-H bonds represents the most straightforward and atom-economical transformation in organic synthesis. An innovative approach integrating photocatalytic hydrogen atom transfer (HAT) and transition metal catalysis has made significant progress in the coupling of α-heterosubstituted C-H bonds with alkyl halides. However, unactivated alkanes were ineffective as a result of the preponderance of byproduct formation. Herein, we demonstrate direct HAT and nickel catalysis in the coupling of cycloalkanes and benzyl bromides/primary alkyl iodides. Additionally, tetrabutylammonium decatungstate (TBADT) was recovered and recycled.
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