Diels-Alder cycloaddition of 4,6-dimethyl-1,2,3-triazine with enamines, ortheir precursors, under microwave irradiation

Authors
Diaz-Ortiz, A de la Hoz, A Prieto, P Carrillo, JR Moreno, A Neunhoeffer, H
Citation
A. Diaz-ortiz et al., Diels-Alder cycloaddition of 4,6-dimethyl-1,2,3-triazine with enamines, ortheir precursors, under microwave irradiation, SYNLETT, (2), 2001, pp. 236-237
Citations number
19
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
2
Year of publication
2001
Pages
236 - 237
Database
ISI
SICI code
0936-5214(200102):2<236:DCO4WE>2.0.ZU;2-Q
Abstract
4,6-Dimethyl-1,2,3-triazine undergoes Diels-Alder cycloaddition with enamin es, derived from cyclic ketones, under microwave irradiation within 20 min. This methodology represents a dramatic improvement on the classical method and allows fused pyridine systems to be obtained, in some cases, in good y ields.