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Synthesis, spectral characterization and biological evaluation of 4H-1,4-benzothiazines, their sulfones and ribofuranosides
2012
European Journal of Chemistry
4H-1,4-Benzothiazines and its derivatives are potential pharmacologically and industrially useful agents. They were prepared by condensation followed by oxidative cyclization of 2-amino-4,6-dimethylbenzenethiol with varied βdiketones/β-ketoesters in dimethyl sulfoxide. On refluxing with H 2 O 2 in glacial acetic acid, the substituted 4H-1,4-Benzothiazines yielded 4H-1,4-Benzothiazine-1,1-dioxides (sulfones). These compounds were evaluated for antioxidant activity by DPPH and ABTS assay and the
doi:10.5155/eurjchem.3.1.106-111.489
fatcat:vrcnhziuijbozox5wi76vlgijq