Issue 33, 2017

Solvent controlled radical cyclization of propargylamines for multi-iodinated quinoline formation

Abstract

A solvent controlled regioselective metal-free synthesis of iodo-substituted N-heterocycles has been developed. This protocol undergoes a cascade iodination/cyclization/oxidation/aromatization pathway to afford multi-halogenated quinolines from readily available propargylamines under mild conditions.

Graphical abstract: Solvent controlled radical cyclization of propargylamines for multi-iodinated quinoline formation

Supplementary files

Article information

Article type
Communication
Submitted
05 Jul 2017
Accepted
31 Jul 2017
First published
31 Jul 2017

Org. Biomol. Chem., 2017,15, 6901-6904

Solvent controlled radical cyclization of propargylamines for multi-iodinated quinoline formation

Y. Zhang, X. Liu, Z. Wu, Y. Wang and Y. Pan, Org. Biomol. Chem., 2017, 15, 6901 DOI: 10.1039/C7OB01637A

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