Manipulation of N,O-Nucleophilicity: Efficient Formation of 4-N-Substituted 2,4-Dihydro-3H-1,2,4-Triazolin-3-ones
Author:
Affiliation:
1. Department of Medicinal Chemistry, Schering-Plough Research Institute, Kenilworth, New Jersey 07033
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0478638
Reference24 articles.
1. Synthesis of certain 1,2,4-triazole nucleoside derivatives
2. Syntheses and structure assignments of six azolinone ribonucleosides
3. 1,2,4-Triazolo[4,3-a]quinoxaline-1,4-diones as antiallergic agents
4. Synthesis of new derivatives of 4-amino-2,4-dihydro-1,2,4-triazol-3-one as potential antibacterial agents
5. Preparation of ribosyl derivatives of 1,2,4-triazol-3(2H)-one and 5-methyl-1,2,4-triazol-3(2H)-one
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1. Transition-metal-free [3 + 2] cycloaddition of C,N-cycloazomethylimines with in situ formed isocyanates from dioxazolones: a facile synthesis of triazolinones;Green Chemistry;2024
2. Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides;Chemical Communications;2015
3. Mechanisms of the cascade synthesis of substituted 4-amino-1,2,4-triazol-3-one from huisgen zwitterion and aldehyde hydrazone: A DFT study;Journal of Computational Chemistry;2012-01-06
4. Five-Membered Heterocycles with Three Heteroatoms: Triazoles;Modern Heterocyclic Chemistry;2011-07-27
5. One pot cascade synthesis of substituted 1,2,4-triazol-3-ones;Chinese Science Bulletin;2010-09
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