Issue 35, 2008
From the journal:

Chemical Communications

From dioxime oxalates to dihydropyrroles and phenanthridines viaiminyl radicals†

Fernando Portela-Cubillo,a   Eoin M. Scanlan,‡a   Jackie S. Scottb  and  John C. Walton*a  

* Corresponding authors

a University of St. Andrews, School of Chemistry, EaStChem, St. Andrews, Fife, UK
E-mail: jcw@st-and.ac.uk
Fax: +44 (0)1334 463808
Tel: +44 (0)1334 463864

b GlaxoSmithKline, New Frontiers Science Park, Third Avenue, Harlow, Essex, UK

Abstract

Dioxime oxalates are useful precursors for the clean generation of iminyl radicals by sensitised UV photolysis and can be adapted for serviceable preparations of 3,4-dihydro-2H-pyrroles and phenanthridines.

Graphical abstract: From dioxime oxalates to dihydropyrroles and phenanthridines viaiminyl radicals

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Article information

DOI
https://doi.org/10.1039/B808625G
Article type
Communication
Submitted
21 May 2008
Accepted
07 Jul 2008
First published
01 Aug 2008

Chem. Commun., 2008, 4189-4191

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From dioxime oxalates to dihydropyrroles and phenanthridines viaiminyl radicals

F. Portela-Cubillo, E. M. Scanlan, J. S. Scott and J. C. Walton, Chem. Commun., 2008, 4189 DOI: 10.1039/B808625G

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