Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry

The electron impact mass spectral fragmentation pathways for a series of 1,3-di- and 1,2,3-trisubstituted imidazolidines were investigated. The data show remarkable differences depending on the location and identity of substituents. The atypical 1,2,2,3-tetrasubstituted imidazolidine, 2-cyano-1- met...

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Autores principales: D'Accorso, Norma Beatriz, Martins Alho, Miriam Amelia
Publicado: 2000
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v37_n1_p57_Salerno
http://hdl.handle.net/20.500.12110/paper_0022152X_v37_n1_p57_Salerno
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spelling paper:paper_0022152X_v37_n1_p57_Salerno2023-06-08T14:46:46Z Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry D'Accorso, Norma Beatriz Martins Alho, Miriam Amelia imidazolidine derivative article chemical reaction chemical structure mass fragmentography mass spectrometry reaction analysis structure analysis The electron impact mass spectral fragmentation pathways for a series of 1,3-di- and 1,2,3-trisubstituted imidazolidines were investigated. The data show remarkable differences depending on the location and identity of substituents. The atypical 1,2,2,3-tetrasubstituted imidazolidine, 2-cyano-1- methyl-3-(p-nitrophenyl)-2-phenylimidazolidine, was also investigated. Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Alho, M.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2000 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v37_n1_p57_Salerno http://hdl.handle.net/20.500.12110/paper_0022152X_v37_n1_p57_Salerno
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic imidazolidine derivative
article
chemical reaction
chemical structure
mass fragmentography
mass spectrometry
reaction analysis
structure analysis
spellingShingle imidazolidine derivative
article
chemical reaction
chemical structure
mass fragmentography
mass spectrometry
reaction analysis
structure analysis
D'Accorso, Norma Beatriz
Martins Alho, Miriam Amelia
Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry
topic_facet imidazolidine derivative
article
chemical reaction
chemical structure
mass fragmentography
mass spectrometry
reaction analysis
structure analysis
description The electron impact mass spectral fragmentation pathways for a series of 1,3-di- and 1,2,3-trisubstituted imidazolidines were investigated. The data show remarkable differences depending on the location and identity of substituents. The atypical 1,2,2,3-tetrasubstituted imidazolidine, 2-cyano-1- methyl-3-(p-nitrophenyl)-2-phenylimidazolidine, was also investigated.
author D'Accorso, Norma Beatriz
Martins Alho, Miriam Amelia
author_facet D'Accorso, Norma Beatriz
Martins Alho, Miriam Amelia
author_sort D'Accorso, Norma Beatriz
title Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry
title_short Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry
title_full Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry
title_fullStr Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry
title_full_unstemmed Spectroscopic analysis of imidazolidines. Part I: Electron impact mass spectrometry
title_sort spectroscopic analysis of imidazolidines. part i: electron impact mass spectrometry
publishDate 2000
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v37_n1_p57_Salerno
http://hdl.handle.net/20.500.12110/paper_0022152X_v37_n1_p57_Salerno
work_keys_str_mv AT daccorsonormabeatriz spectroscopicanalysisofimidazolidinespartielectronimpactmassspectrometry
AT martinsalhomiriamamelia spectroscopicanalysisofimidazolidinespartielectronimpactmassspectrometry
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