Sign in
DOUBLE INTRAMOLECULAR 1,3-DIPOLAR CYCLOADDITION OF DIAZIDO-TERMINAL DIALKYNE: SYNTHESIS OF A NEW BIS(1,2,3-TRIAZOLO-1,4-OXAZINE)
Journal article   Peer reviewed

DOUBLE INTRAMOLECULAR 1,3-DIPOLAR CYCLOADDITION OF DIAZIDO-TERMINAL DIALKYNE: SYNTHESIS OF A NEW BIS(1,2,3-TRIAZOLO-1,4-OXAZINE)

Nejib Husein Mekni and Ahmed Baklouti
Heterocycles, Vol.85(7), pp.1727-1733
01/07/2012

Abstract

Chemistry Chemistry, Organic Physical Sciences Science & Technology
A new bis(1,2,3-triazolo-1,4-oxazine) fused heterocyclic compound was synthesized from terminal meso-1,2,3,4-diepoxybutane via azide ring opening reaction, followed by propargylation and double 1,3-dipolar intramolecular cycloaddition. No effect on the reaction outcome was observed when Cu(I) was used as catalyst. In both cases catalyzed and uncatalyzed reactions, only the exo-tetracyclic two to two fused isomer was obtained.

Metrics

1 Record Views

Details