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dc.contributor.author | Chugunova E. | |
dc.contributor.author | Samsonov V. | |
dc.contributor.author | Akylbekov N. | |
dc.contributor.author | Mazhukin D. | |
dc.date.accessioned | 2018-09-19T22:00:06Z | |
dc.date.available | 2018-09-19T22:00:06Z | |
dc.date.issued | 2017 | |
dc.identifier.issn | 0040-4020 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/144574 | |
dc.description.abstract | © 2017 Elsevier LtdThe synthesis of novel 2H-benzimidazole 1,3-dioxides on the basis of o-benzoquinone dioximes interaction with ketones in the presence of acids is described. Nitration of these compounds by nitric acid in acetic acid yields the 5-nitro derivatives of 2H-benzimidazole 1,3-dioxide. | |
dc.relation.ispartofseries | Tetrahedron | |
dc.subject | 2H-benzimidazole 1,3-dioxide | |
dc.subject | Ketone | |
dc.subject | Nitration | |
dc.subject | o-Benzoquinone dioxime | |
dc.subject | Separase inhibitor | |
dc.title | Synthesis of 2H-benzimidazole 1,3-dioxides, separase inhibitors, by reaction of o-benzoquinone dioximes with ketones | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 27-28 | |
dc.relation.ispartofseries-volume | 73 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 3986 | |
dc.source.id | SCOPUS00404020-2017-73-2728-SID85019708401 |