Issue 18, 2016

Straightforward synthesis of functionalized chroman-4-ones through cascade radical cyclization-coupling of 2-(allyloxy)arylaldehydes

Abstract

A novel and direct approach to synthesize a series of phosphonate, azide and hydroxy functionalized chroman-4-ones has been developed. The cascade transformation appears to proceed through an intramolecular addition of an in situ generated acyl radical onto the alkene, followed by a selective nucleophilic radical–electrophilic radical cross coupling.

Graphical abstract: Straightforward synthesis of functionalized chroman-4-ones through cascade radical cyclization-coupling of 2-(allyloxy)arylaldehydes

Supplementary files

Article information

Article type
Communication
Submitted
25 Nov 2015
Accepted
01 Feb 2016
First published
01 Feb 2016

Chem. Commun., 2016,52, 3661-3664

Straightforward synthesis of functionalized chroman-4-ones through cascade radical cyclization-coupling of 2-(allyloxy)arylaldehydes

J. Zhao, P. Li, X. Li, C. Xia and F. Li, Chem. Commun., 2016, 52, 3661 DOI: 10.1039/C5CC09730D

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