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Synthesis and properties of azoles and their derivatives.23. Electron impact mass spectrometry of regio- and stereoisomeric diarylnitroisoxazolines

Published

Author(s)

Anzor I. Mikaia, Andre Baranski

Abstract

General fragmentation pathways for nitro-substituted di(aryl)isoxazolines under electron ionization are determined. Ions useful for differentiation of positional and stereo-isomers are established.
Citation
Chemistry of Heterocyclic Compounds
Volume
26
Issue
1

Keywords

Mass spectra, electron ionization, isoxazolines, Fragmentation mechanism

Citation

Mikaia, A. and Baranski, A. (1990), Synthesis and properties of azoles and their derivatives.23. Electron impact mass spectrometry of regio- and stereoisomeric diarylnitroisoxazolines, Chemistry of Heterocyclic Compounds, [online], https://doi.org/10.1007/BF00506854 (Accessed October 28, 2025)

Issues

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Created January 1, 1990, Updated January 27, 2020
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