化学
立体选择性
烯烃纤维
催化作用
试剂
键裂
药物化学
钴
劈理(地质)
立体化学
组合化学
有机化学
断裂(地质)
工程类
岩土工程
作者
Ye Lim Kim,Sun-a Park,Seoung‐Mi Choi,Jong‐Un Park,Ju Hyun Kim
出处
期刊:Organic Letters
[American Chemical Society]
日期:2021-08-16
卷期号:23 (17): 6674-6679
被引量:10
标识
DOI:10.1021/acs.orglett.1c02219
摘要
An atom-economical strategy for the C–H alkenylation and C–H allylation of arenes by employing cyclopropenes as versatile alkenylating and allylating reagents is reported, catalyzed by cobalt. The Co-catalyzed C–H alkenylation process involves sequential C–H and C–C bond cleavage. Under the optimized conditions, broad-ranging alkenylated (hetero)arenes were synthesized with complete (E)-stereoselectivity (up to 91%). The consecutive C–H allylation proved viable under basic conditions via double-bond migration of the initially generated alkenyl (hetero)arenes, thus leading to allylated (hetero)arenes with high stereoselectivity of olefin (E/Z ratio = 91:9 to 100:0).
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