芳基
化学
区域选择性
质子化
插入反应
基质(水族馆)
反应条件
组合化学
药物化学
立体化学
有机化学
催化作用
海洋学
地质学
离子
作者
Xiaojin Li,Yuping Sun,Xin Huang,Lei Zhang,Lichun Kong,Bo Peng
出处
期刊:Organic Letters
[American Chemical Society]
日期:2017-02-03
卷期号:19 (4): 838-841
被引量:59
标识
DOI:10.1021/acs.orglett.6b03840
摘要
The aryne insertion into “S═O” bond has been validated recently. This technology is elusively applied to the synthesis of thioethers. In contrast to the reported cases, the reaction described furnished o-aryloxy triarylsulfonium salts, in lieu of thioethers, in good to excellent yields. The reaction is also featured by its exquisite regioselectivity, broad substrate scope, and mild conditions (25 °C). Preliminary mechanistic studies suggest that the reaction probably proceeds in a sequential [2 + 2] cycloaddtion/O-arylation/protonation pathway.
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