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史蒂文斯-绍梅莱特-豪泽重排反应的机制。理论研究。

The mechanism of the Stevens and Sommelet-Hauser rearrangements. A theoretical study.

机构信息

Dipartimento di Chimica Generale e Chimica Organica, C. so M. d'Azeglio 48, I-10125 Torino, Italy.

出版信息

J Org Chem. 2010 Jun 4;75(11):3608-17. doi: 10.1021/jo100367z.

Abstract

The [1,2] and [2,3] migration steps in the Stevens and Sommelet-Hauser rearrangements which occur in the ylides of quaternary ammonium salts have been studied at M05-2x levels. The Stevens migration has been found to take place through a diradical pathway in several cases (tetramethylammonium, benzyltrimethylammonium, benzylphenacyldimethylammonium ylides). By contrast, in the phenyltrimethylammonium ylide this reaction takes place through a concerted process. The Sommelet-Hauser rearrangement takes place through a concerted transition structure. The most important factor determining the extent of competition with the Stevens rearrangement is the difference in the reaction energies as the formation of the Sommelet-Hauser intermediate is significantly less endoergic.

摘要

[1,2]和[2,3]迁移步骤在季铵盐的叶立德中发生的Stevens 和Sommelet-Hauser 重排中已在 M05-2x 水平上进行了研究。在几种情况下(四甲基铵、苄基三甲基铵、苄基苯甲酰基二甲基铵叶立德),发现Stevens 迁移是通过自由基途径发生的。相比之下,在苯基三甲基铵叶立德中,该反应是通过协同过程发生的。Sommelet-Hauser 重排是通过协同过渡态进行的。决定与Stevens 重排竞争程度的最重要因素是反应能的差异,因为Sommelet-Hauser 中间体的形成明显不那么内禀能。

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