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

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

Output data

Year: 1998, Volume: 34, Number: 3, Pages: 271-274 Pages count : DOI: 10.1007/BF02290715

Authors

Samsonov V. A. , Volodarskii L. B.

Affiliations

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

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.

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

Published print:

Mar 1, 1998

Scopus	2-s2.0-27544488853
Elibrary	13282862
OpenAlex	W1992522080