Fragmentation pathways arising from protonation at different sites in aminoalkyl-substituted 3-hydroxy-1,2,5-oxadiazoles (3-hydroxyfurazans)
Author:
Affiliation:
1. Department of Chemistry; Dalhousie University; 6274 Coburg Road, PO Box 15000 Halifax Nova Scotia B3H 4R2 Canada
2. Dipartimento di Scienza e Tecnologia del Farmaco (DSTF); Università degli Studi di Torino; via Pietro Giuria 9 10125 Torino Italy
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Analytical Chemistry
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Tandem mass spectrometry of homologous 3‐hydroxyfurazan and nitrile amino acids: Analysis of cooperative interactions and fragmentation processes;Journal of Mass Spectrometry;2024-05-24
2. Structure Study of Proton Tautomers Based on Ion Mobility Mass Spectrometry and Ab Initio Molecular Dynamics Calculations;CHINESE J ANAL CHEM;2024
3. Intramolecular interactions and the neutral loss of ammonia from collisionally activated, protonated ω-aminoalkyl-3-hydroxyfurazans;European Journal of Mass Spectrometry;2023-11-17
4. Fragmentation reactions of protonated α,ω‐diamino carboxylic acids: The importance of functional group interactions;Journal of Mass Spectrometry;2021-06-13
5. Hydroxyazoles as acid isosteres and their drug design applications—Part 1: Monocyclic systems;Advances in Heterocyclic Chemistry;2021
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