Reaction of 1-substituted 3,5-diamino-1,2,4-triazoles with β-keto esters: synthesis and new rearrangement of mesoionic 3-amino-2H-[1,2,4]triazolo-[4,3-a]pyrimidin-5-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Enhancing the Anticancer Potential of Targeting Tumor-Associated Metalloenzymes via VEGFR Inhibition by New Triazolo[4,3-a]pyrimidinone Acyclo C-Nucleosides Multitarget Agents;Molecules;2022-04-08
2. Type A mesoionic compounds (1980–2020);Advances in Heterocyclic Chemistry;2022
3. Structure-based design and optimization of pyrimidine- and 1,2,4-triazolo[4,3-a]pyrimidine-based matrix metalloproteinase-10/13 inhibitors via Dimroth rearrangement towards targeted polypharmacology;Bioorganic Chemistry;2020-03
4. Advances on Synthesis and Biological Activities of Mesoionic Compounds;Chinese Journal of Organic Chemistry;2020
5. Facile and regioselective synthesis of new fluorinated [1,2,4]-triazolo[4,3-a]pyrimidin-7(1H)-one derivatives from fluorinated alkynes;Journal of Fluorine Chemistry;2020-01
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