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喹啉衍生的NNP-锰配合物催化酮与伯醇的α-烷基化反应。

Quinoline-derived NNP-manganese complex catalyzed α-alkylation of ketones with primary alcohols.

作者信息

Song Peidong, Rong Haojie, Meng Tingting, Cui Zhe, Mao Mingzhen, Yang Cuifeng

机构信息

Xi'an Modern Chemistry Research Institute, Xi'an 710065, China.

出版信息

Org Biomol Chem. 2024 Jun 26;22(25):5112-5116. doi: 10.1039/d4ob00827h.

Abstract

An air-stable quinoline-derived NNP ligand chelated Mn catalyst was developed for the efficient α-alkylation of ketones with primary alcohols a hydrogen auto-transfer methodology. The sole by-product formed is water, rendering the protocol atom efficient. A wide range of ketone and alcohol substrates were employed, providing the α-alkylated ketones with isolated yields up to 94%. This system was also efficient for the green synthesis of quinoline derivatives while using (2-aminophenyl)methanol as an alkylating reagent.

摘要

开发了一种空气稳定的喹啉衍生的NNP配体螯合锰催化剂,用于通过氢自动转移方法使酮与伯醇进行高效的α-烷基化反应。形成的唯一副产物是水,使该方法具有原子经济性。使用了多种酮和醇底物,得到的α-烷基化酮的分离产率高达94%。当使用(2-氨基苯基)甲醇作为烷基化试剂时,该体系对于喹啉衍生物的绿色合成也很有效。

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