2-ALKOXYCARBONYLCYCLOIMMONIUM YLIDES, EFFICIENT 1,4-DIPOLE EQUIVALENTS IN THE SYNTHESIS OF NEW CONJUGATED BETAINES

Authors
CUADRO AM VALENCIANO J VAQUERO JJ NAVIO JLG ALVAREZBUILLA J
Citation
Am. Cuadro et al., 2-ALKOXYCARBONYLCYCLOIMMONIUM YLIDES, EFFICIENT 1,4-DIPOLE EQUIVALENTS IN THE SYNTHESIS OF NEW CONJUGATED BETAINES, Tetrahedron, 49(15), 1993, pp. 3185-3192
Citations number
12
Journal title
Tetrahedron → ACNP
ISSN journal
00404020
Volume
49
Issue
15
Year of publication
1993
Pages
3185 - 3192
Database
ISI
SICI code
0040-4020(1993)49:15<3185:2YE1E>2.0.ZU;2-W
Abstract
Several heterocyclic mesomeric betaines containing the bicyclic system s pyrido[1,2-a]pyrazine and pyrido [2,1-f][1,2,4]triazine have been pr epared by reaction of 2-alkoxycarbonyl pyridinium N-ylides with phenyl isocyanate and isothiocyanate.