Issue 10, 2000
From the journal:

Chemical Communications

Intramolecular 1,3-dipolar cycloadditions of 2-substituted norbornadiene-tethered nitrones

Geoffrey K. Tranmer,a   Peter Keecha  and  William Tam*a  

* Corresponding authors

a Guelph-Waterloo Centre for Graduate Work in Chemistry and Biochemistry, Department of Chemistry and Biochemistry, University of Guelph, Guelph, Ontario, Canada
E-mail: tam@chembio.uoguelph.ca

Abstract

Efficient routes for the synthesis of norbornadiene-tethered nitrones have been developed and their intramolecular 1,3-dipolar cycloadditions were found to be highly regio- and stereo-selective.

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Article information

DOI
https://doi.org/10.1039/B001543L
Article type
Communication
Submitted
24 Feb 2000
Accepted
31 Mar 2000
First published
05 May 2000

Chem. Commun., 2000, 863-864

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Intramolecular 1,3-dipolar cycloadditions of 2-substituted norbornadiene-tethered nitrones

G. K. Tranmer, P. Keech and W. Tam, Chem. Commun., 2000, 863 DOI: 10.1039/B001543L

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