Mikaia, A.
, Trusova, E.
, Perepelitchenko, L.
and Zaikin, V.
(1980),
Effects of stereoisomerism in the mass spectra of 2,4-disubstituted thiacyclohexanes, Chemistry of Heterocyclic Compounds, [online], https://doi.org/10.1007/BF00505985
(Accessed July 17, 2024)
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.
Effects of stereoisomerism in the mass spectra of 2,4-disubstituted thiacyclohexanes
Published
Author(s)
, Elena Trusova, Lyudmila Perepelitchenko, Vladimir G. Zaikin
Abstract
The stereospecificity of fragmentation for isomeric dialkyl- and methyl,phenylthiacyclohexanes under electron ionization are established. Experimentally obtained relative Ionization and appearance energies for the stereoisomers are in agreement with fragmentation mechanisms.Citation
Chemistry of Heterocyclic Compounds
Volume
17
Issue
3
Pub Type
Journals
Download Paper
Keywords
Mass spectra, Ionization energy, Appearance energy, Thiacyclohexanes, Fragmentation mechanism
Citation
Issues
If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.
Created July 9, 1980, Updated November 10, 2018