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通过催化剂控制的 2-乙烯基苯胺和炔酸酯的串联环化反应合成 C2-取代的喹啉和吲哚的 C-C 键断裂。

Cleavage of C-C Bonds for the Synthesis of C2-Substituted Quinolines and Indoles by Catalyst-Controlled Tandem Annulation of 2-Vinylanilines and Alkynoates.

机构信息

State Key Laboratory of Applied Organic Chemistry, Department of Chemistry , Lanzhou University , Gansu , China.

School of Chemistry and Chemical Engineering , Yangtze Normal University , Chongqing , China.

出版信息

Org Lett. 2018 Mar 16;20(6):1534-1537. doi: 10.1021/acs.orglett.8b00260. Epub 2018 Mar 8.

Abstract

The strategy for the synthesis of C2-substituted indoles and quinolines from 2-vinylanilines and alkynoates through C-C bond cleavage is developed. With these general methods, 2-substituted indoles and quinolines can be accessed via tandem Michael addition and cyclization with no requirement of oxidant. This strategy not only provides a method for the synthesis C2-substituted indoles in good yields through the simultaneous cleavage of C═C and C≡C bonds under metal-free conditions but also provides a simple method for the generation of the C2-substituted quinolines in moderate yields via Pd-catalyzed C≡C bond cleavage.

摘要

开发了一种通过 C-C 键断裂,由 2-乙烯基苯胺和炔酸酯合成 C2-取代吲哚和喹啉的策略。使用这些通用方法,可以通过串联迈克尔加成和环化反应,无需氧化剂,来获得 2-取代的吲哚和喹啉。该策略不仅提供了一种在无金属条件下通过同时断裂 C═C 和 C≡C 键以高产率合成 C2-取代吲哚的方法,而且还提供了一种通过 Pd 催化的 C≡C 键断裂以中等产率生成 C2-取代喹啉的简单方法。

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