化学
区域选择性
氧化还原
催化作用
亲核细胞
草酸盐
烷基
激进的
有机化学
亲核加成
组合化学
药物化学
作者
Wenhui Sun,Jian‐Yu Zou,xiao-jing xu,Jinlin Wang,mei-ling liu,Xue-Yuan Liu
标识
DOI:10.1002/adsc.202200310
摘要
Abstract Difunctionalization of alkenes enables construction of complex compounds in one pot. In this report, we presented an intermolecular, redox‐neutral three‐component dicarbofunctionalization of activated alkenes under mild reaction conditions. The mechanistic studies indicated tertiary alkyl radicals from oxalate salts were first added to alkenes in Giese‐type fashion, followed by nucleophilic addition with aldehydes to produce the desired 1,2‐dialkylation products. The catalyst system does not require any additives, with good functional group compatibility, regioselectivity, and constructs two tertiary carbon centers simultaneously. magnified image
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