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Synthesis and properties of azoles and their derivatives.25. Electron impact mass spectra of nitro- and nitroalkyl-substituted 3-aryl-isoxazolines.

Published

Author(s)

Anzor I. Mikaia, Andre Baranski

Abstract

It is determined that dissociation of molecular ions of aryl-isoxazolines under electron ionization takes place primarily through the nitro- and halogen-containing groups. Detailed analysis of the most important fragmentation pathways are presented
Citation
Chemistry of Heterocyclic Compounds
Volume
26
Issue
7

Keywords

Mass spectra, electron ionization, Fragmentation, isoxazolines, “Mass spectra” ”, ”electron ionization”, “Fragmentation” ”, ”isoxazolines”, “Mass spectra” ”, ”electron ionization”, “Fragmentation” ”, ”isoxazolines”, “Mass spectra” ”, ”electron ionization”, “Fragmentation” ”, ”isoxazolines”

Citation

Mikaia, A. and Baranski, A. (1990), Synthesis and properties of azoles and their derivatives.25. Electron impact mass spectra of nitro- and nitroalkyl-substituted 3-aryl-isoxazolines., Chemistry of Heterocyclic Compounds, [online], https://doi.org/10.1007/BF00509716 (Accessed December 10, 2024)

Issues

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Created September 1, 1990, Updated January 27, 2020