An Efficient Route to Ethyl 5-Alkyl- (Aryl)-1H-1,2,4-triazole-3-carboxylates
Author:
Affiliation:
1. Biotechnology and Bionanotechnology Department; Lomonosov Moscow University of Fine Chemical Technology; Vernadskogo pr. 86 Moscow Russian Federation
Funder
Russian Foundation for Basic Research
State Contract
Publisher
Wiley
Subject
Organic Chemistry
Reference11 articles.
1. A convenient synthesis of 3,5-disubstituted-1,2,4-triazoles
2. Rapid Synthesis of 1,3,5-Substituted 1,2,4-Triazoles from Carboxylic Acids, Amidines, and Hydrazines
3. The Chemistry of 1,2,4-Triazoles.
4. Improved routes to methyl 4-methylimidazole-2-carboxylate and methyl 5-methyl-1,2,4-triazole-3-carboxylate
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1. Chemo-enzymatic synthesis of 5-substituted ribavirin analogs: Unexpected cooperative effect in the interaction of 5-alkyloxymethyl 1,2,4-triazol-3-carboxamides with E. coli purine nucleoside phosphorylase active site;Sustainable Chemistry and Pharmacy;2022-12
2. Synthesis of 5-oxymethyl-1,2,4-triazole-3-carboxamides;Fine Chemical Technologies;2022-09-30
3. Expanding the chemical space of 3(5)-functionalized 1,2,4-triazoles;Chemistry of Heterocyclic Compounds;2022-02
4. Chemo-Enzymatic Synthesis of 5-Substituted Ribavirin Analogs: Unexpected Cooperative Effect in the Interaction of 5-Alkyloxymethyl 1,2,4-Triazol-3-Carboxamides with <i>E. Coli</i> Purine Nucleoside Phosphorylase Active Site;SSRN Electronic Journal;2022
5. 5‐Substituted 1,2,4‐Triazole‐3‐Carboxylates and 5‐Substituted Ribavirin Analogs Synthesis;Current Protocols;2021-11
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