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Rh(III)-催化级联环化反应生成 -乙酰链的螺吡咯并异喹啉衍生物。

Rh(III)-Catalyzed cascade annulation to produce an -acetyl chain of spiropyrroloisoquinoline derivatives.

机构信息

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

出版信息

Org Biomol Chem. 2022 Mar 16;20(11):2293-2299. doi: 10.1039/d2ob00137c.

Abstract

A new rhodium(III)-catalyzed multistep cascade spirocyclization approach was developed to synthesize a novel -acetyl chain of spiropyrroloisoquinoline derivatives using oxadiazoles as the directing group. This one-pot reaction also isolates aryloxadiazole derivatives as cross-coupling intermediates. This simple approach could efficiently expand the scope of the skeletons of isoquinolines and aryloxadiazoles.

摘要

发展了一种新的铑(III)催化多步级联螺环化方法,使用恶二唑作为导向基团,合成了新型螺吡咯异喹啉衍生物的 -乙酰链。该一锅反应还分离出芳基恶二唑衍生物作为交叉偶联中间体。这种简单的方法可以有效地扩展异喹啉和芳基恶二唑骨架的范围。

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