Gas‐phase fragmentation of protonated 3‐phenoxy imidazo[1,2‐a] pyridines using tandem mass spectrometry and computational chemistry
Author:
Affiliation:
1. College of Chemistry, The Key Laboratory of Chemical Biology and Organic Chemistry of Henan Province Zhengzhou University Zhengzhou China
2. Institute of Drug Discovery Technology Ningbo University Ningbo China
Funder
National Natural Science Foundation of China
Publisher
Wiley
Subject
Spectroscopy
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jms.4794
Reference49 articles.
1. Base- and Ligand-free Room-Temperature Synthesis of N-Fused Heteroaromatic Compounds via the Transition Metal-Catalyzed Cycloisomerization Protocol
2. Novel selenylated imidazo[1,2-a]pyridines for breast cancer chemotherapy: Inhibition of cell proliferation by Akt-mediated regulation, DNA cleavage and apoptosis
3. Structure‐based design and synthesis of imidazo[1,2‐a]pyridine derivatives as novel and potent Nek2 inhibitors with in vitro, and in vivo antitumor activities;Xi JB;Eur J Med Chem,2016
4. Imidazo[1,2- a ]Pyridine-3-Carboxamides Are Active Antimicrobial Agents against Mycobacterium avium Infection In Vivo
5. Discovery of a new series of imidazo[1,2-a]pyridine compounds as selective c-Met inhibitors
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