区域选择性
重氮
化学
四唑
组合化学
烷基化
催化作用
相容性(地球化学)
功能群
卡宾
有机化学
化学工程
聚合物
工程类
作者
Shunhua Zhou,Chunyan Li,Jie Zhang,Jian Lyu,Jie Liao,Haifeng Wang,Qiongjiao Yan,Shuang‐Xi Gu
标识
DOI:10.1021/acs.joc.4c00531
摘要
Regioselective methods to access alkylated tetrazoles still remain a challenging goal. Herein, we describe a novel regioselective protocol for N2-arylation of tetrazoles with diazo compounds using inexpensive Al(OTf)3. This reaction could be conducted under mild conditions to access a diverse array of alkylated tetrazoles with 2-substituted tetrazoles as the major products, demonstrating a comprehensive range of substrate compatibility and excellent functional group compatibility. Mechanistic studies revealed a carbene-free process in this reaction procedure. Furthermore, the scale-up reaction and transformations of the N2-arylation of tetrazole products demonstrated the potential of this strategy.
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