Chemical ribosylation of 5-substituted 1,2,4-triazole-3-carboxylates
Author:
Affiliation:
1. Moscow Politechnical University, Moscow, Russia;
2. Lomonosov Institute of Fine Chemical Technologies, Moscow Technological University, Moscow, Russia;
3. Moscow Institute of Physics and Technology (State University), Dolgoprudny, Russia
Funder
Ministry of Education and Science of the Russian Federation
Publisher
Informa UK Limited
Subject
Genetics,Molecular Medicine,Biochemistry,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/15257770.2019.1576881
Reference24 articles.
1. Bioactive nucleoside analogues possessing selected five-membered azaheterocyclic bases
2. Triazole Nucleoside Derivatives Bearing Aryl Functionalities on the Nucleobases Show Antiviral and Anticancer Activity
3. Chemoenzymatic method of 1,2,4-triazole nucleoside synthesis: Possibilities and limitations
4. Novel 5-alkyl(aryl)-substituted ribavirine analogues: synthesis and antiviral evaluation
5. An alternative route to the arylvinyltriazole nucleosides
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3. 5‐Substituted 1,2,4‐Triazole‐3‐Carboxylates and 5‐Substituted Ribavirin Analogs Synthesis;Current Protocols;2021-11
4. Parallel synthesis of derivatives of 1H-1,2,4-triazole-3-carboxylic acids with heterocyclic substituents at position 5;Chemistry of Heterocyclic Compounds;2020-09
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