> A concise indium(III)‐catalyzed annulation of 2,3‐disubstituted indoles with o ‐aminobenzyl alcohols is reported. The in situ ge'/> Concise Synthesis of Polycyclic Indoline Scaffolds through an In <sup xmlns='http://www.wiley.com/namespaces/wiley'>IIIIII ‐Catalyzed Formal [4+2] Annulation of 2,3‐Disubstituted Indoles with <i xmlns='http://www.wiley.com/namespaces/wiley'>oo ‐Aminobenzyl Alcohols
首页> 外文期刊>European journal of organic chemistry >Concise Synthesis of Polycyclic Indoline Scaffolds through an In IIIIII ‐Catalyzed Formal [4+2] Annulation of 2,3‐Disubstituted Indoles with oo ‐Aminobenzyl Alcohols
【24h】

Concise Synthesis of Polycyclic Indoline Scaffolds through an In IIIIII ‐Catalyzed Formal [4+2] Annulation of 2,3‐Disubstituted Indoles with oo ‐Aminobenzyl Alcohols

机译:通过在 iii III中简明综合合成多环吲哚氏脚手架 - 催化形式[4 + 2]的2,3-二取代的 具有 o o-aminobenzyl醇的indoles

获取原文
获取原文并翻译 | 示例
           

摘要

> A concise indium(III)‐catalyzed annulation of 2,3‐disubstituted indoles with o ‐aminobenzyl alcohols is reported. The in situ generated aza‐ ortho ‐quinone methides (aza‐ o QMs) were efficiently trapped by diverse carbazoles in a formal [4+2] cycloaddition reaction catalyzed by indium(III) triflate, which provided rapid access to bridged polycyclic indoline alkaloid skeletons.
机译: >一个简洁的铟(iii) - 催化2,3-二取代吲哚的催化剂 o < / i>据报道 - 氨基苄醇。 原位生成的AZA- 邻rOTHO - 醌甲基(AZA- QMS)被铟催化的正式[4 + 2]环加成反应中的不同的咔唑有效地捕获了各种咔唑( III)Triflate提供了快速进入桥接多环吲哚碱基骨骼骨架。

著录项

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号