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 | ||
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| Output data | Year: 1997, Volume: 33, Number: 3, Pages: 343-345 Pages count : DOI: 10.1007/BF02253116 | ||
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                            Abstract:
                            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.
                        
                    
                
                        Cite:
                                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 OpenAlex
                    
                    
                                            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 OpenAlex
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                    | Published print: | Mar 1, 1997 | 
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                | Scopus: | 2-s2.0-27544498048 | 
| Elibrary: | 13274187 | 
| OpenAlex: | W2053494183 |