Issue 42, 2020

Site-selective halogenation on meso-mesityl substituents of 10,20-dimesityl-5,15-diazaporphyrins with an AuX3/AgOTf combination

Abstract

We have developed site-selective bromination on the mesityl substituents of 10,20-dimesityl-5,15-diazaporphyrins. Treatment of 10,20-dimesityl-5,15-diazaporphyrin and its nickel(II) complex with a combination of AuBr3/AgOTf induced selective bromination on the mesityl groups. These brominated products can be employed for late-stage modification of the aryl substituents.

Graphical abstract: Site-selective halogenation on meso-mesityl substituents of 10,20-dimesityl-5,15-diazaporphyrins with an AuX3/AgOTf combination

Supplementary files

Article information

Article type
Communication
Submitted
04 Aug 2020
Accepted
04 Oct 2020
First published
05 Oct 2020

Dalton Trans., 2020,49, 14786-14789

Site-selective halogenation on meso-mesityl substituents of 10,20-dimesityl-5,15-diazaporphyrins with an AuX3/AgOTf combination

J. Longevial, K. Miyagawa and H. Shinokubo, Dalton Trans., 2020, 49, 14786 DOI: 10.1039/D0DT02727H

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