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Analyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydes

Authordc.contributor.authorNúñez Vergara, Luis es_CL
Authordc.contributor.authorNavarrete Encina, Patricio es_CL
Authordc.contributor.authorSalas, S. es_CL
Authordc.contributor.authorConde, B. es_CL
Authordc.contributor.authorCarbajo, J. es_CL
Authordc.contributor.authorSquella Serrano, Juan es_CL
Authordc.contributor.authorCamargo Grandón, Rodrigo 
Admission datedc.date.accessioned2008-08-28T15:38:44Z
Available datedc.date.available2008-08-28T15:38:44Z
Publication datedc.date.issued2007-05-09
Cita de ítemdc.identifier.citationJOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS 44(1):236-242en
Identifierdc.identifier.issn0731-7085
Identifierdc.identifier.urihttp://repositorio.uchile.cl/handle/2250/120473
Abstractdc.description.abstractEl mass spectra of products of the dihydropyridine Hantzsch synthesis using hydroxy and methoxy aldehydes as starting materials are reported. The reaction products (C-4 hydroxy- and methoxyphenyl-1,4-dihydropyridines and chromeno[3,4,c]-pyridines) were derivatized with N-methyl-N-(trimethylsilyl)-trifluoracetamide to be analyzed by gas chromatographic techniques. Fragmentation pathways for 1,4-dihydropyridines and chromeno-pyridines are proposed. The study provides (mainly through MS-MS technique) useful data for the confirmation of the structure of the compounds and also is a valuable tool for further analytical purposes to follow both photostability and reactivity studies with free radicals for these types of compounds.en
Lenguagedc.language.isoenen
Publisherdc.publisherPERGAMON-ELSEVIER SCIENCEen
Keywordsdc.subjectGC-MSen
Títulodc.titleAnalyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydesen
Document typedc.typeArtículo de revistaen


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