Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow 226001, India.
J Org Chem. 2013 Jul 5;78(13):6769-74. doi: 10.1021/jo400799b. Epub 2013 Jun 21.
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.
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。