Investigation of short lived radicals in aromatic nucleophilic substitution by use of nitroso compounds as scavengers

I. I. Bilkis*, S. M. Shein

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

Radical intermediates formed in reaction of substituted nitrobenzene compounds with nucleophilic reagents have been trapped by t-nitrosobutane to yield nitroxide radicals which have been characterized in situ by ESR. The formation of short-lived radicals originating from reagents and solvents has been shown.

Original languageEnglish
Pages (from-to)969-971
Number of pages3
JournalTetrahedron
Volume31
Issue number8
DOIs
StatePublished - 1975
Externally publishedYes

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