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

Published

Author(s)

Anzor I. 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 April 23, 2024)
Created April 1, 1986, Updated January 27, 2020