化学
卤化物
分子内力
催化作用
赫克反应
烷基
β-氢化物消除
钯
选择性
组合化学
药物化学
有机化学
作者
Long Shu,Xu Dong,Ze‐Hua Sun,A. Zhao,Mengyao Jiang,Ren Xiao-Min,Fachao Yan,Kai Cao,Qing Liu,Hui Liu
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-06-28
卷期号:26 (27): 5719-5724
被引量:1
标识
DOI:10.1021/acs.orglett.4c01821
摘要
A novel photocatalytic palladium-induced 6-endo-selective alkyl Heck reaction of unactivated alkyl iodides and alkyl bromides has been described. This strategy facilitates the gentle and efficient synthesis of a variety of 5-phenyl-1,2,3,6-tetrahydropyridine derivatives. It demonstrates a broad substrate tolerance and excellent 6-endo selectivity. Unlike the high-temperature requirements of traditional alkyl Heck reactions, this transformation efficiently proceeds at room temperature and shows significant promise for industrial-scale applications. Mechanistic investigations reveal that this alkyl Heck reaction proceeds via a hybrid palladium–radical process.
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