Issue 5, 2000

Enhanced radical delivery from aldoxime esters for EPR and ring closure applications

Abstract

Arylmethaniminyl and alkyl radicals were generated from di- and tri-methoxyphenyl aldoxime esters, by photolysis in the presence of 4-methoxyacetophenone, and were detected by EPR spectroscopy: good yields of cyclised products were isolated from suitably unsaturated alkyl substituents.

Article information

Article type
Communication
Submitted
24 Dec 1999
Accepted
26 Jan 2000
First published
21 Feb 2000

Chem. Commun., 2000, 351-352

Enhanced radical delivery from aldoxime esters for EPR and ring closure applications

A. J. McCarroll and J. C. Walton, Chem. Commun., 2000, 351 DOI: 10.1039/A910346P

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