Issue 41, 2018

Tandem radical cyclization of N-methacryloyl benzamides with CBr4 to construct brominated isoquinolinediones

Abstract

A simple cumene (isopropylbenzene, IPB) promoted auto-oxidation involved tandem radical cyclization of N-methacryloyl benzamides using stable and easy-to-handle CBr4 as the bromine source is described. This strategy provides an efficient and practical approach for the synthesis of bromine containing isoquinolinediones. This method also presents a new way to generate bromine radicals using a mild auto-oxidation pathway.

Graphical abstract: Tandem radical cyclization of N-methacryloyl benzamides with CBr4 to construct brominated isoquinolinediones

Supplementary files

Article information

Article type
Paper
Submitted
11 Aug 2018
Accepted
01 Oct 2018
First published
02 Oct 2018

Org. Biomol. Chem., 2018,16, 7748-7752

Tandem radical cyclization of N-methacryloyl benzamides with CBr4 to construct brominated isoquinolinediones

S. Huang, P. Niu, Y. Su, D. Hu and C. Huo, Org. Biomol. Chem., 2018, 16, 7748 DOI: 10.1039/C8OB01964A

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