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铼催化酚类与内炔的区域选择性邻位烯基化反应及[3 + 2 + 1]环加成反应

Rhenium-Catalyzed Regioselective ortho-Alkenylation and [3 + 2 + 1] Cycloaddition of Phenols with Internal Alkynes.

作者信息

Murai Masahito, Yamamoto Masaki, Takai Kazuhiko

机构信息

Division of Applied Chemistry, Graduate School of Natural Science and Technology , Okayama University , 3-1-1 Tsushimanaka, Kita-ku , Okayama 700-8530 , Japan.

出版信息

Org Lett. 2019 May 3;21(9):3441-3445. doi: 10.1021/acs.orglett.9b01214. Epub 2019 Apr 18.

Abstract

An operationally simple and direct rhenium-catalyzed ortho-alkenylation ( C-alkenylation) of unprotected phenols with alkynes was developed. The protocol provided ortho-alkenylphenols exclusively, and formation of para- or multiply alkenylated phenols and hydrophenoxylation ( O-alkenylation) products were not observed. The [3 + 2 + 1] cycloaddition of phenols and two alkynes via ortho-alkenylation was also demonstrated, in which the alkynes functioned as both two- and one-carbon units. These reactions proceeded with readily available starting materials under neutral conditions without additional ligands.

摘要

开发了一种操作简单直接的铼催化未保护酚与炔烃的邻位烯基化反应(C-烯基化反应)。该方法仅提供邻位烯基酚,未观察到对位或多烯基化酚以及氢酚氧基化(O-烯基化)产物的形成。还证明了通过邻位烯基化反应酚与两个炔烃的[3 + 2 + 1]环加成反应,其中炔烃同时作为双碳单元和单碳单元。这些反应在中性条件下使用容易获得的起始原料进行,无需额外的配体。

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