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 |
|