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钯(II)催化邻芳基苯胺与炔烃的[5+2]氧化环化反应高立体选择性合成含亚胺的二苯并[b,d]氮杂卓

Highly Stereoselective Synthesis of Imine-Containing Dibenzo[b,d]azepines by a Palladium(II)-Catalyzed [5+2] Oxidative Annulation of o-Arylanilines with Alkynes.

机构信息

Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of the Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi'an, 710069 (China).

出版信息

Angew Chem Int Ed Engl. 2015 Dec 14;54(51):15385-9. doi: 10.1002/anie.201508850. Epub 2015 Nov 2.

Abstract

A novel palladium(II)-catalyzed [5+2] oxidative annulation of readily available o-arylanilines with alkynes has been developed for building a seven-membered N-heterocyclic architecture containing a biaryl linkage. This method is applicable to a wide range of unprotected o-arylanilines and internal alkynes, and results in the chemoselective preparation of imine-containing dibenzo[b,d]azepines in high yields with excellent diastereoselectivity with respect to the two types of stereogenic elements.

摘要

一种新型的钯(II)催化的[5+2]氧化环加成反应,可将易得的邻芳基苯胺与炔烃反应,构建含有联苯结构的七元 N-杂环体系。该方法适用于广泛的未保护的邻芳基苯胺和内部炔烃,以高产率和优异的非对映选择性合成了含有亚胺的二苯并[b,d]氮杂卓。

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