Analyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydes
Abstract
EI 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. © 2007.
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Título según WOS: | Analyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydes |
Título según SCOPUS: | Analyses by GC-MS and GC-MS-MS of the hantzsch synthesis products using hydroxy- and methoxy-aromatic aldehydes |
Título de la Revista: | JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS |
Volumen: | 44 |
Número: | 1 |
Editorial: | Elsevier |
Fecha de publicación: | 2007 |
Página de inicio: | 236 |
Página final: | 242 |
Idioma: | English |
URL: | http://linkinghub.elsevier.com/retrieve/pii/S0731708507000647 |
DOI: |
10.1016/j.jpba.2007.01.025 |
Notas: | ISI, SCOPUS |