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.

Mass spectrometric study of 1,2,4- and 1,3,4-oxadiazoles containing indole substituents.

Published

Author(s)

Anzor Mikaia, Rosa Ushakova, Vladimir G. Zaikin, VI Kelarev, GA Shveikhgeimer

Abstract

Under electron ionization major fragmentation pathways for indolyloxadiazoles proceed via cleavage of C-O, C-N and N-O bonds in the oxadiazole ring. Skeletal rearrangements due to a migration of aryl groups are detected for diaryl1,3,4-oxadiazoles.
Citation
Chemistry of Heterocyclic Compounds
Volume
22
Issue
4

Keywords

Mass spectra, Electron ionization, Fragmentation, Oxadiazole

Citation

Mikaia, A. , Ushakova, R. , Zaikin, V. , Kelarev, V. and Shveikhgeimer, G. (1986), Mass spectrometric study of 1,2,4- and 1,3,4-oxadiazoles containing indole substituents., Chemistry of Heterocyclic Compounds, [online], https://doi.org/10.1007/BF00542788 (Accessed May 22, 2026)
Additional citation formats

Issues

If you have any questions about this publication or are having problems accessing it, please contact [email protected].

Created April 1, 1986, Updated May 7, 2026
Was this page helpful?