Formation of derivatives of benzofuran, indole, and cinnoline in the reaction of 7-(N-morpholinyl)-7-methyl-8a-hydroxy-4,5,8,8a-tetrahydro-7H-pyrrolo[3,2-e]-2,1, 3-benzoxadiazole 6-oxide with nucleophilic reagents Full article
| Journal | Chemistry of Heterocyclic Compounds ISSN: 0009-3122 , E-ISSN: 1573-8353 | ||
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| Output data | Year: 1998, Volume: 34, Number: 3, Pages: 271-274 Pages count : DOI: 10.1007/BF02290715 | ||
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                            Abstract:
                            7-(N-Morpholinyl)-7-methyl-8a-hydroxy-4,5,8,8a-tetrahydro-7H-pyrrolo[3,2 -e] -2,1,3-benzoxadiazole 6-oxide behaves as the synthetic equivalent of a 1,4-dicarbonyl compound in reactions with amines, dioxime, and hydrazine to give derivatives of benzofuran, indole, 1,4-dioxime, and pyridazine. This compound also undergoes reactions characteristic for nitrones, adding water and a hydride ion. ©1998 Plenum Publishing Corporation.
                        
                    
                
                        Cite:
                                Samsonov V.A.
    ,        Volodarskii L.B.
    
Formation of derivatives of benzofuran, indole, and cinnoline in the reaction of 7-(N-morpholinyl)-7-methyl-8a-hydroxy-4,5,8,8a-tetrahydro-7H-pyrrolo[3,2-e]-2,1, 3-benzoxadiazole 6-oxide with nucleophilic reagents
Chemistry of Heterocyclic Compounds. 1998. V.34. N3. P.271-274. DOI: 10.1007/BF02290715 Scopus РИНЦ OpenAlex
                    
                    
                                            Formation of derivatives of benzofuran, indole, and cinnoline in the reaction of 7-(N-morpholinyl)-7-methyl-8a-hydroxy-4,5,8,8a-tetrahydro-7H-pyrrolo[3,2-e]-2,1, 3-benzoxadiazole 6-oxide with nucleophilic reagents
Chemistry of Heterocyclic Compounds. 1998. V.34. N3. P.271-274. DOI: 10.1007/BF02290715 Scopus РИНЦ OpenAlex
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                    | Published print: | Mar 1, 1998 | 
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                                            | Scopus: | 2-s2.0-27544488853 | 
| Elibrary: | 13282862 | 
| OpenAlex: | W1992522080 | 
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