Methyl 4-hydroxy-2-methyl-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide
4-Hydroxy-1-methyl-2(1H)-quinolone was used as nucleophile in electrochemical oxidation of catechols and the reaction was studied by cyclic voltammetry and controlled-potential coulometry[1]. It was used in ceric ammonium nitrate-mediated oxidative cycloaddition of 1,3-dicarbonyls to conjugated compounds to yield substituted dihydrofurans, dihydrofurocoumarins, dihydrofuroquinolinones and dihydrofurophenalenones[2]. It was used in the synthesis of :
• 3-(4-methoxybenzyl)-4-h
• 3-(benzo[d][1,3]dioxol-5-ylmethyl)-
• 3-(4-chlorobenzyl)-4-hy
• 3,3′-bis(4-chlorobenzylidene)-1,1
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