Issue 38, 2016

Intramolecular 1,5-H transfer reaction of aryl iodides through visible-light photoredox catalysis: a concise method for the synthesis of natural product scaffolds

Abstract

The intramolecular 1,5-H transfer reaction of the aryl radicals generated from unactivated aryl iodides by photocatalysis is described. The features of this transformation are operational simplicity, excellent yields, mild reaction conditions, and good functional group tolerance. With this approach, a more concise formal synthesis of (±)-coerulescine and (±)-physovenine is accomplished.

Graphical abstract: Intramolecular 1,5-H transfer reaction of aryl iodides through visible-light photoredox catalysis: a concise method for the synthesis of natural product scaffolds

Supplementary files

Article information

Article type
Communication
Submitted
07 Mar 2016
Accepted
11 Apr 2016
First published
13 Apr 2016

Chem. Commun., 2016,52, 6455-6458

Intramolecular 1,5-H transfer reaction of aryl iodides through visible-light photoredox catalysis: a concise method for the synthesis of natural product scaffolds

J. Chen, Y. Wei, G. Xu, Y. Liang and P. Xu, Chem. Commun., 2016, 52, 6455 DOI: 10.1039/C6CC02007K

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