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噻蒽氧化物介导的芳烃的选择性硅烷化反应。

Site-Selective Silylation of Arenes Mediated by Thianthrene -Oxide.

机构信息

State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, CAS, 345 Lingling Road, Shanghai 200032, China.

CAS Key Laboratory of Energy Regulation Materials, Shanghai Institute of Organic Chemistry, CAS, 345 Lingling Road, Shanghai 200032, China.

出版信息

Org Lett. 2020 Aug 21;22(16):6657-6661. doi: 10.1021/acs.orglett.0c02458. Epub 2020 Aug 10.

Abstract

The thianthrene -oxide (TTSO)-mediated site-selective silylation of arenes has been realized via a thianthrenation/Pd-catalyzed silylation sequence. This method features a broad substrate scope and wide functional group tolerance under mild conditions and allows the synthesis of a set of (hetero)arylsilanes with operationally simple manipulations. The application and generality of the approach were further demonstrated by the late-stage functionalization of marketed drugs. This reaction also represents the first example of a Pd-catalyzed silylation reaction of aryl sulfonium salts.

摘要

通过噻蒽氮化物/钯催化的硅烷化序列,实现了噻蒽氧化物(TTSO)介导的芳基的选择性硅烷化。该方法在温和条件下具有广泛的底物范围和宽的官能团容忍度,并允许通过操作简单的操作合成一系列(杂)芳基硅烷。该方法的应用和通用性通过对市售药物的后期功能化进一步得到证明。该反应也是芳基锍盐的钯催化硅烷化反应的第一个例子。

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