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金催化的炔基氮丙啶环化反应是一种高效构建功能化 N-苯并吡咯的方法。

Gold-catalyzed cyclization of alkynylaziridines as an efficient approach toward functionalized N-phth pyrroles.

机构信息

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Lu, Shanghai 200032, People's Republic of China.

出版信息

J Org Chem. 2010 Jan 15;75(2):510-3. doi: 10.1021/jo902357x.

Abstract

An efficient access to N-phth pyrrroles via gold-catalyzed cycloisomerization of N-phth alkynylaziridines has been described. Functionalized pyrroles including pyrrole-2-carboxylates or 2-pyrrolyl ketone are easily constructed in generally good yields by this method. The resulting pyrroles can be further converted to N-amino pyrrole or 2-acyl pyrrole, which are important synthetic intermediates for amplification of molecular complexity.

摘要

通过金催化的 N-苯炔基氮丙啶环异构化反应,可以有效地合成 N-苯并吡咯。该方法通常可以高产率构建各种功能化的吡咯,包括吡咯-2-羧酸酯或 2-吡咯基酮。所得的吡咯可以进一步转化为 N-氨基吡咯或 2-酰基吡咯,它们是分子复杂性扩增的重要合成中间体。

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