Journal of the Chemical Society. Perkin transactions I p. 543 - 546 (1989)
Update date:2022-08-03
Topics:
Boulton
Devi, Purabi
Henderson, Neil
Jarrar, Adil A.
Kiss, Miklos
3-Substituted 1,2,3-benzotriazin-4(3H)-one 1-oxides are formed on peracid oxidation of 3-alkyl- and 3-methoxy-1,2,3-benzotriazin-4(3H)-ones. The 3-(a-alkoxyalkyl) 1-oxide derivatives could be dealkylated to the tautomeric 3-unsubstituted compound. The acidities of the isomeric N-oxides of the 1,2,3-benzotriazinone system are compared. Phenyl iodosodiacetate converts o-nitrobenzaldehyde benzyl- and phenyl-hydrazones into the 2-substituted 4-oxido-1,2,3-benzotriazine1 -oxide betaines(1).
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Doi:10.1134/S1070363209060395
(2009)Doi:10.1016/S0040-4039(00)82133-4
(1988)Doi:10.1021/ja910462x
(2010)Doi:10.1021/ja9103638
(2010)Doi:10.1016/j.cclet.2009.09.002
(2010)Doi:10.1016/S0040-4039(01)80615-8
(1989)
