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通过分子内 Wittig 反应,使用酯、硫酯和酰胺制备功能化苯并呋喃、苯并噻吩和吲哚。

Preparation of functional benzofurans, benzothiophenes, and indoles using ester, thioester, and amide via intramolecular Wittig reactions.

机构信息

Department of Chemistry, National Taiwan Normal University, Taipei, Taiwan, ROC.

出版信息

Org Lett. 2011 Jun 3;13(11):2970-3. doi: 10.1021/ol201062r. Epub 2011 May 12.

Abstract

Preparation of new types of highly functional benzofurans, benzothiophenes, and indoles is realized via intramolecular Wittig reactions with the corresponding ester, thioester, and amide functionalities. The key intermediates, phosphorus ylides, presumably result from the addition of Bu(3)P toward aldehydes followed by acylation and deprotonation. Synthesis of functional benzofurans directly starting from salicylic aldehyde derivatives with acid chlorides in a one-step procedure is also developed.

摘要

通过与相应酯、硫酯和酰胺官能团的分子内 Wittig 反应,实现了新型高官能度苯并呋喃、苯并噻吩和吲哚的制备。推测关键中间体磷叶立德是通过向醛中添加 Bu(3)P 后进行酰化和去质子化反应得到的。还开发了一种从水杨醛衍生物和酰氯一步法直接合成功能化苯并呋喃的方法。

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