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C-N 和 C-O 亲电试剂的还原偶联。

Reductive Coupling between C-N and C-O Electrophiles.

机构信息

State Key Laboratory of Applied Organic Chemistry (SKLAOC), College of Chemistry and Chemical Engineering , Lanzhou University , 222 South Tianshui Road , Lanzhou 730000 , China.

出版信息

J Am Chem Soc. 2019 Aug 14;141(32):12481-12486. doi: 10.1021/jacs.9b05224. Epub 2019 Aug 1.

Abstract

The cross-electrophile reaction is a promising strategy for C-C bond formation. Recent studies have focused mainly on reactions with organic halides. Here we report a coupling reaction between C-N and C-O electrophiles that demonstrates the possibility of constructing a C-C bond via C-N and C-O cleavage. Several reactions between benzyl/aryl ammonium salts and vinyl/aryl C-O electrophiles have been studied. Preliminary mechanistic studies revealed that the benzyl ammoniums were activated through a radical mechanism.

摘要

交叉亲电反应是一种形成 C-C 键的很有前途的策略。最近的研究主要集中在与有机卤化物的反应上。在这里,我们报告了 C-N 和 C-O 亲电试剂之间的偶联反应,该反应证明了通过 C-N 和 C-O 的断裂构建 C-C 键的可能性。研究了几种苄基/芳基铵盐和乙烯基/芳基 C-O 亲电试剂之间的反应。初步的机理研究表明,苄基铵通过自由基机理活化。

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