oxazole


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ox·a·zole

(ok'să-zōl),
The fundamental ring system of pyranoses.
References in periodicals archive ?
Synthesis of some new Schiff bases containing thiazole and oxazole nuelei and their fungieidal aetivity.
Tenders are invited for Supply of freshly prepared scintillation grade 2,5 di phenyl oxazole (ppo, c15h11no)
The physiological functions of GA are usually moderated via nonionic mechanisms such as N-methyl-D-aspartate (NMDA), A-amino-hydroxy methyl oxazole propionic acid, kainic acid receptor and metabolic GA receptor.
The ester was reacted without purification and immediately treated with ammonium acetate in acetic acid to generate oxazole 4 (45% overall).
The relative importance of the planar fused ring(s) versus the nature of the aromatic ring substituted at the oxazole two position on the pi-radical reactivity toward a weak proton donor is investigated and discussed.
129) Use: additive Use: herbicide Class: carboxylic acid Class: amide, oxazole 18 FD&C Yellow 6 1,4-Diaminoanthraquinone [2783-94-0] [128-95-0] (score = 0.
The modular and convergent method of the oxazole synthesis will facilitate both major and fine tuning of the catalysts function in single point, dual point and triple point activation, across nucleophilic catalysis, H-bond activation, and secondary amine catalysis for iminium and enamine based processes.
The researchers started with a compound called an oxazole.
1-2]Phenacyl bromides are of particular important molecules because they are widely used as precursors of various pharmaceutically important heteroaromatics such as imidazoles, selenazoles, and oxazoles.
Performance analysis of neural network models for oxazolines and oxazoles derivatives descriptor dataset, International Journal of Information Sciences and Techniques (IJIST) 3(6): 1-15.
Scala, "A new construction of diversely functionalized oxazoles from enolizable cyclic 1,3-dicarbonyls and 5(4H)-oxazolones," Synlett, no.
This eventually produces many important classes of flavour compounds including furans, pyrazines, pyrroles, oxazoles, thiophenes, thiazoles and other heterocyclic compounds (Figure 5; Melton, 1999).