4.6 Article

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

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 16, Issue 41, Pages 7748-7752

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ob01964a

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Funding

  1. National Natural Science Foundation of China [21562037]

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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.

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