New applications of westphal condensation. Synthesis of new [2.3.3]cyclazinones

Authors
Pastor Fernández, Joaquín; Matía Martín, Ma de la Paz; García Navío, José LuisUniversity of Alcalá Author; Vaquero López, Juan J.; Álvarez-Builla Gómez, JulioUniversity of Alcalá Author
Identifiers
Permanent link (URI): http://hdl.handle.net/10017/3698
DOI: 10.3987/COM-89-5172
ISSN: 1881-0942
Publisher
The Japan Institute of Heterocyclic Chemistry Publications
Date
1989
Affiliation
Universidad de Alcalá. Departamento de Química Orgánica
Funders
Comisión Asesora de Investigación Científica y Técnica-CAICYT
Bibliographic citation
Heterocycles, 1989, v.29, n.12, p.2369-2377
Keywords
Westphal Condensation
[2.3.3]cyclazinone isomers
Document type
info:eu-repo/semantics/article
Version
info:eu-repo/semantics/publishedVersion
Publisher's version
http://dx.doi.org/10.3987/COM-89-5172
Rights
© The Japan Institute of Heterocyclic Chemistry, 1989
Access rights
info:eu-repo/semantics/openAccess
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Abstract
Two different types of [2.3.3]cyclazinone isomers were obtained by methods based on the Westphal condensation. 2,6-Dialkylpyridinium salts were condensed with 1,2-acenaphtenequinone to produce [2.3.3]cyclazin-1-one derivatives. By a similar process, a quinolizinium-1-olate was prepared, which was cyclized with DMAD yielding a [2.3.3]cyclazin-6-one derivative.
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