Unexpected formation of a substituted furazano-[3,4-d]pyridazine trioxide from α-hydroxylamino-aldoxime and its photochemical conversion to a pyrrolidine nitroxyl radical

Unexpected formation of a substituted furazano-[3,4-d]pyridazine trioxide from α-hydroxylamino-aldoxime and its photochemical conversion to a pyrrolidine nitroxyl radical Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 1997, Volume: 33, Number: 3, Pages: 343-345 Pages count : DOI: 10.1007/BF02253116

Authors

Mazhukin D. G. , Tikhonov A. Ya. , Petrenko O. P. , Volodarskii L. B.

Affiliations

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, 630090 Novosibirsk, Russian Federation

The oxidation of 2-hydroxyamino-2-methylpropanaldoxime by NaOBr leads to 4,4,7,7,-tetramethyl-4,7-dihydrofurazano[3,4-d]pyridazine 1,5,6-trioxide, which is converted upon photolysis to 4,4,6,6-tetramethyl-4,6-dihydropyrrolo[3,4-c]furazane 1-oxide 5-oxyl. ©1997 Plenum Publishing Corporation.

Mazhukin D.G. , Tikhonov A.Y. , Petrenko O.P. , Volodarskii L.B.
Unexpected formation of a substituted furazano-[3,4-d]pyridazine trioxide from α-hydroxylamino-aldoxime and its photochemical conversion to a pyrrolidine nitroxyl radical
Chemistry of Heterocyclic Compounds. 1997. V.33. N3. P.343-345. DOI: 10.1007/BF02253116 Scopus РИНЦ

Published print:

Mar 1, 1997

Scopus	2-s2.0-27544498048
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