A Copper-Catalyzed Arylation of Tryptamines for the Direct Synthesis of Aryl Pyrroloindolines.

A Copper-Catalyzed Arylation of Tryptamines for the Direct Synthesis of Aryl Pyrroloindolines.
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DOI:
10.1039/c2sc20914d
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发表时间:
2012-11
期刊:
影响因子:
8.4
通讯作者:
Reisman SE
Reisman SE
中科院分区:
化学1区
文献类型:
--
作者:
Kieffer ME;Chuang KV;Reisman SE

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操作简单,铜催化的n -甲基色胺的芳基化提供了直接获得c3 -芳基吡咯啉的途径。吲哚主链和芳基亲电试剂上都能容忍一系列供电子和吸电子取代基。这些反应在环境温度下发生,偶联物的量等摩尔。
An operationally simple, copper-catalyzed arylation of N-tosyltryptamines provides direct access to C3-aryl pyrroloindolines. A range of electron-donating and electron-withdrawing substituents is tolerated on both the indole backbone and the aryl electrophile. These reactions occur under ambient temperatures and with equimolar quantities of the coupling partners.