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Authordc.contributor.authorQuiroga, Jairo 
Authordc.contributor.authorHormaza, Angelina 
Authordc.contributor.authorInsuasty, Braulio 
Authordc.contributor.authorSaitz Barría, Claudio 
Authordc.contributor.authorJullian Matthaei, Carolina 
Authordc.contributor.authorCañete, Alvaro 
Admission datedc.date.accessioned2018-12-20T15:04:09Z
Available datedc.date.available2018-12-20T15:04:09Z
Publication datedc.date.issued1998
Cita de ítemdc.identifier.citationJournal of Heterocyclic Chemistry, Volumen 35, Issue 1, 1998, Pages 61-64
Identifierdc.identifier.issn0022152X
Identifierdc.identifier.other10.1002/jhet.5570350112
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/157463
Abstractdc.description.abstractA series of pyrazolo[1,5-a]pyrimidin-3-ones 3 was prepared from Meldrum's acid and 5-amino-3-arylpyrazoles 1 by cyclization in nitrobenzene of the corresponding 5-pyrazolylaminomethylene Meldrum's acid derivatives 2. The structure of pyrazolo[1,5-a]pyrimidin-3-ones and their precursors were determined by nmr measurements.
Lenguagedc.language.isoen
Publisherdc.publisherHeteroCorporation
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceJournal of Heterocyclic Chemistry
Keywordsdc.subjectOrganic chemistry
Títulodc.titleSynthesis of pyrazolo[1,5-a]pyrimidines in the reaction of 5-amino- 3-arylpyrazoles with methoxymethylene meldrum's acid derivatives and thermolysis of their pyrazolylaminomethylene derivatives
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorrvh
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile