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铜(II)催化吲哚 C3-H 酯基直接加成反应的,-双齿辅助基团

Copper(II)-catalysed direct C3-H esterification of indoles assisted by an ,-bidentate auxiliary moiety.

机构信息

College of Pharmaceutical Sciences, Zhejiang University, 866 Yuhangtang Rd., Hangzhou, Zhejiang 310058, China.

出版信息

Org Biomol Chem. 2021 May 5;19(17):3911-3924. doi: 10.1039/d0ob02301a.

Abstract

The regioselective direct C3-esterification of indoles with OXA is developed in an efficient reaction with carboxylic acids using the catalyst CuBr2 and oxidants Ag2CO3 and K2S2O8. The simple experimental procedure is proved to be broadly applicable to a range of substrates, including aromatic and aliphatic acids, and the corresponding products were obtained in good yields up to 87%. At the same time, it provides a valuable approach to produce C3-benzyl derivatives of indoles through reaction with benzyl carboxylic acid under the same reaction conditions.

摘要

发展了一种使用催化剂 CuBr2 和氧化剂 Ag2CO3 和 K2S2O8,通过羧酸对吲哚进行区域选择性直接 C3-酯化的有效反应。简单的实验程序被证明广泛适用于一系列底物,包括芳香酸和脂肪酸,并以高达 87%的良好收率得到相应的产物。同时,它提供了一种通过在相同反应条件下与苯甲酸反应来制备吲哚 C3-苄基衍生物的有价值的方法。

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