烷基化
化学
重氮
选择性
催化作用
光化学
金属
组合化学
有机化学
作者
Jingya Yang,Jiaokui Duan,Ganggang Wang,Hongyan Zhou,Ben Ma,Chengqi Wu,Jianliang Xiao
出处
期刊:Organic Letters
[American Chemical Society]
日期:2020-09-09
卷期号:22 (18): 7284-7289
被引量:53
标识
DOI:10.1021/acs.orglett.0c02619
摘要
A visible-light-promoted highly site-selective N1-alkylation of benzotriazoles with diazo compounds has been achieved under mild and metal-free conditions. Using cheap, readily available p-benzoquinone (PBQ) as a catalyst, a wide range of benzotriazoles and diazo compounds are reacted, providing N1-alkylated benzotriazoles in moderate to excellent yields with excellent N1-selectivities. Preliminary mechanistic studies suggest that a radical process accounts for the exclusive site-selectivity of this transformation.
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