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金催化的连续炔烃活化:通过炔烃/6-endo-内型碳环化反应的级联氢芳化一锅法合成 NH-咔唑。

Gold-catalyzed sequential alkyne activation: one-pot synthesis of NH-carbazoles via cascade hydroarylation of alkyne/6-endo-dig carbocyclization reactions.

机构信息

Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow 226001, India.

出版信息

J Org Chem. 2013 Jul 5;78(13):6769-74. doi: 10.1021/jo400799b. Epub 2013 Jun 21.

Abstract

A simple and efficient one-pot protocol for the synthesis of NH-carbazoles has been described. The strategy comprises a one-pot reaction involving the treatment of 2-alkynyl indoles with arylacetylenes in the presence of an Au-Ag combination catalyst. The salient feature of the strategy involves sequential activation of terminal and internal alkynes leading to the cascade hydroarylation of terminal alkynes and 6-endo-dig carbocyclization reactions. The generality of the method has been demonstrated by using a series of 2-alkynyl indoles and arylacetylenes.

摘要

已描述了一种合成 NH-咔唑的简单高效一锅法。该策略包括一锅反应,涉及在 Au-Ag 组合催化剂存在下用芳基乙炔处理 2-炔基吲哚。该策略的突出特点包括末端炔烃和内部炔烃的顺序活化,导致末端炔烃的级联氢芳化和 6-endo-dig 碳环化反应。该方法的通用性已通过一系列 2-炔基吲哚和芳基乙炔得到证明。

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