Advancements in visible-light-induced reactions via alkenyl radical intermediates

被引:3
|
作者
Piedra, Helena F. [1 ,2 ,3 ]
Plaza, Manuel [1 ,2 ,3 ]
机构
[1] Univ Oviedo, Dept Quim Organ & Inorgan, Julian Claveria 8, Oviedo 33006, Spain
[2] Univ Oviedo, Inst Univ Quim Organometal Enr Moles, Julian Claveria 8, Oviedo 33006, Spain
[3] Univ Oviedo, Ctr Innovac Quim Avanzada ORFEO CINQA, Julian Claveria 8, Oviedo 33006, Spain
关键词
ALPHA-BROMOCHALCONES; MONOFLUOROALKENYLATION; CYCLIZATION; CATALYSIS; ARYL;
D O I
10.1007/s43630-024-00580-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In recent years, visible-light-induced organic transformations have taken a central role driving forward the progress of modern organic synthesis. These processes typically involve the transient generation of highly reactive radical intermediates, facilitating a diverse array of chemical reactions. Despite the abundance of synthetic strategies enabling the access of aryl and alkyl-centered radicals, the exploitation of photochemistry to generate highly reactive alkenyl radicals has remained notably underdeveloped. In this review, we present recent advancements in visible-light-induced transformations that proceed through the generation of alkenyl radicals from alkenyl-containing precursors, predominantly alkenyl halides, showcasing their application in various organic transformations.
引用
收藏
页码:1217 / 1228
页数:12
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