Jump to main content
Jump to site search

Issue 41, 2006
Previous Article Next Article

Ring opening and ring closure in an indolizine structure activated through SNAr coupling with superelectrophilic 4,6-dinitrobenzofuroxan, an unusual intramolecular oxygen transfer from a N-oxide functionality

Author affiliations

Abstract

Coupling of superelectrophilic 4,6-dinitrobenzofuroxan with a π-excessive indolizine structure affords a strongly dipolar substitution product which undergoes a facile but unusual rearrangement induced by an intramolecular oxygen atom transfer from the N-oxide functionality of the DNBF moiety.

Graphical abstract: Ring opening and ring closure in an indolizine structure activated through SNAr coupling with superelectrophilic 4,6-dinitrobenzofuroxan, an unusual intramolecular oxygen transfer from a N-oxide functionality

Back to tab navigation

Supplementary files

Article information


Submitted
13 Jun 2006
Accepted
24 Jul 2006
First published
01 Sep 2006

Chem. Commun., 2006, 4279-4281
Article type
Communication

Ring opening and ring closure in an indolizine structure activated through SNAr coupling with superelectrophilic 4,6-dinitrobenzofuroxan, an unusual intramolecular oxygen transfer from a N-oxide functionality

S. Kurbatov, A. Tatarov, V. Minkin, R. Goumont and F. Terrier, Chem. Commun., 2006, 4279
DOI: 10.1039/B608350A

Social activity

Search articles by author

Spotlight

Advertisements