Issue 1, 2017, Issue in Progress

Transition metal- and organophotocatalyst-free perfluoroalkylation reaction of amino(hetero)aromatics initiated by the complex [(TMEDA)I·I3] and visible light

Abstract

Radical initiation for the perfluoroalkylation reaction of amino(hetero)aromatics has been accomplished employing the complex [(TMEDA)I·I3] and visible light. This methodology circumvents the use of metal(organo)catalysts and biologically-relevant substrates are easily substituted with RF moieties employing a mild and environmentally benign radical strategy starting from readily-available perfluoroalkyl iodides RFI.

Graphical abstract: Transition metal- and organophotocatalyst-free perfluoroalkylation reaction of amino(hetero)aromatics initiated by the complex [(TMEDA)I·I3] and visible light

Supplementary files

Article information

Article type
Paper
Submitted
05 Oct 2016
Accepted
16 Nov 2016
First published
03 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 266-274

Transition metal- and organophotocatalyst-free perfluoroalkylation reaction of amino(hetero)aromatics initiated by the complex [(TMEDA)I·I3] and visible light

D. E. Yerien, R. Conde, S. Barata-Vallejo, B. Camps, B. Lantaño and A. Postigo, RSC Adv., 2017, 7, 266 DOI: 10.1039/C6RA24786E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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