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无外加光催化剂的可见光促进吲哚嗪的合成。

External-Photocatalyst-Free Visible-Light-Mediated Synthesis of Indolizines.

机构信息

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149 Münster (Germany) http://www.uni-muenster.de/Chemie.oc/glorius/

Organisch-Chemisches Institut, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149 Münster (Germany) http://www.uni-muenster.de/Chemie.oc/glorius/.

出版信息

Angew Chem Int Ed Engl. 2015 Dec 14;54(51):15545-9. doi: 10.1002/anie.201506868. Epub 2015 Nov 4.

Abstract

A visible-light-mediated synthesis of valuable polycyclic indolizine heterocycles from easily accessed brominated pyridine and enol carbamate derivatives has been developed. This process, which operates at room temperature under irradiation from readily available light sources, does not require the addition of an external photocatalyst. Instead, an investigation into the reaction mechanism indicates that the indolizine products themselves may be in some way involved in mediating and accelerating their own formation. Preliminary studies also show that these simple heterocyclic compounds may be capable of facilitating other visible-light-mediated transformations.

摘要

可见光促进的从易得的溴代吡啶和烯醇碳酸酯衍生物合成有价值的多环吲哚嗪杂环已经被开发出来。这个过程在室温下进行,在易得的光源照射下进行,不需要添加外部光催化剂。相反,对反应机制的研究表明,吲哚嗪产物本身可能以某种方式参与介导和加速它们的形成。初步研究还表明,这些简单的杂环化合物可能能够促进其他可见光介导的转化。

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