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铁催化串联氧化偶联和缩醛水解反应制备甲酰化苯并噻唑和异喹啉。

Iron-catalyzed tandem oxidative coupling and acetal hydrolysis reaction to prepare formylated benzothiazoles and isoquinolines.

机构信息

College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang, Jiangxi 330022, P. R. China.

出版信息

Chem Commun (Camb). 2021 Apr 4;57(26):3271-3274. doi: 10.1039/d1cc00621e. Epub 2021 Mar 2.

Abstract

The aldehyde group is one of the most versatile intermediates in synthetic chemistry, and the introduction of an aldehyde group into heteroarenes is important for the transformation of molecular structure. Herein, we achieved the direct formylation of benzothiazo/les and isoquinolines. The reaction features a novel iron-catalyzed Minisci-type oxidative coupling process using commercially available 1,3-dioxolane as a formylated reagent followed by acetal hydrolysis without a separation process. The reaction can be performed under exceedingly mild reaction conditions and exhibits broad functional group tolerance.

摘要

醛基是合成化学中最通用的中间体之一,在杂芳烃中引入醛基对于分子结构的转化非常重要。在此,我们实现了苯并噻唑/苯并异喹啉和异喹啉的直接甲酰化。该反应采用新型铁催化的 Minisci 型氧化偶联过程,使用商业上可获得的 1,3-二氧戊环作为甲酰化试剂,然后进行缩醛水解,无需分离过程。反应可以在非常温和的反应条件下进行,并具有广泛的官能团容忍度。

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