Catalytic trifluoromethylation of uracil to 5-trifluoromethyluracil by use of CF3I and its industrial applications
Author:
Publisher
Elsevier BV
Subject
Process Chemistry and Technology,Catalysis
Reference37 articles.
1. The term of “5-trifluoromethyluracil” should be “5-trifluoromethylpyridine-2,4(1H,3H)-dion followed by the nomenclature of IUPAC. Expediently, we named the products obtained here as the substituted uracils. The systematic names of g and l are mentioned in 4. 5.
2. Synthesis and Pharmacological Characterization of N3-Substituted Willardiine Derivatives: Role of the Substituent at the 5-Position of the Uracil Ring in the Development of Highly Potent and Selective GLUK5 Kainate Receptor Antagonists
3. 5-(Trifluoromethyl)-β-l-2′-deoxyuridine, the l-Enantiomer of Trifluorothymidine: Stereospecific Synthesis and Antiherpetic Evaluations
4. Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii
5. Structure-activity relationship of nucleobase ligands of uridine phosphorylase from Toxoplasma gondii
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