Skip to main content
U.S. flag

An official website of the United States government

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

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 June 21, 2024)

Issues

If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.

Created September 1, 1990, Updated January 27, 2020