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铑催化通过 N-磺酰基-1,2,3-三唑与 2-羟基苄醇的 Transannulation 合成苯并吡喃。

Rhodium Catalyzed Synthesis of Benzopyrans via Transannulation of N-Sulfonyl-1,2,3-triazoles with 2-Hydroxybenzyl Alcohols.

机构信息

Department of Chemistry , Indian Institute of Technology Madras , Chennai 600036 , India.

出版信息

Org Lett. 2018 Jul 6;20(13):3762-3765. doi: 10.1021/acs.orglett.8b01338. Epub 2018 Jun 20.

Abstract

An efficient and novel rhodium-catalyzed transannulation of N-sulfonyl-1,2,3-triazoles with in situ generated o-quinone methides ( o-QMs) from 2-hydroxybenzyl alcohols has been achieved for the synthesis of substituted benzopyrans in good yields. The developed reaction involves nucleophilic attack of o-QM to α-imino rhodium carbenoid to generate a carbonyl ylide followed by 6π-electrocyclization and isomerization. Furthermore, the utility of the methodology was demonstrated in the one-pot synthesis and construction of polyheteroaromatics.

摘要

一种高效、新颖的铑催化 N-磺酰基-1,2,3-三唑与 2-羟基苄醇原位生成的邻醌甲醚(o-QMs)的transannulation 反应已经实现,用于合成取代的苯并吡喃,产率良好。所开发的反应涉及 o-QM 对α-亚氨基铑卡宾的亲核攻击,生成羰基叶立德,然后进行 6π-电环化和异构化。此外,该方法的实用性在一锅法合成和多杂芳烃的构建中得到了证明。

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