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Synthesis of Pyrrolo[1,2-a]indoles via (3+2)-Annulations of (Aza)-para-Quinone Methides with Indoles
Synthesis ( IF 2.2 ) Pub Date : 2020-08-04 , DOI: 10.1055/s-0040-1707348
Xiang-Zhi Zhang 1 , Bao Qiong Li 1 , Zong-Wang Qiu 1 , Gui-Hua Wen 1 , Ai-Jun Ma 1 , Peng-Jin Bao 1 , Ji-Yuan Du 2 , Xue-Tao Xu 1 , Na Feng 1
Affiliation  


Abstract

An efficient and straightforward Brønsted acid mediated (3+2)-annulation of (aza)-para-quinone methides, generated in situ from propargylic alcohols and indoles, has been developed involving 1,8-conjugate addition/5-endo annulation cascade. This protocol affords a mild and effective method for the construction of synthetically important and structurally interesting functionalized pyrrolo[1,2-a]indoles.



中文翻译:

通过(3 + 2)-(Aza)-对-醌醌甲基吲哚的(3 + 2)合成吡咯并[1,2-a]吲哚


摘要

介导的高效和简单的布朗斯台德酸(3 + 2)的(氮杂)-annulation --quinone甲基化物,从炔丙醇和吲哚在原位产生的,已经开发了涉及1,8-共轭加成/ 5-内切环级联。该协议提供了一种温和而有效的方法,用于构建具有重要合成意义的重要结构化吡咯并[1,2- a ]吲哚。

更新日期:2020-08-05
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