dc.contributor.author |
Fedotova N. |
|
dc.contributor.author |
Litvinov I. |
|
dc.contributor.author |
Kataeva O. |
|
dc.date.accessioned |
2018-09-17T21:16:57Z |
|
dc.date.available |
2018-09-17T21:16:57Z |
|
dc.date.issued |
1994 |
|
dc.identifier.issn |
1066-5285 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/134779 |
|
dc.description.abstract |
Novel arylsulfonylureas were prepared by the reaction of chloroacetyl isocyanate with arylsulfamides. The structures of the compounds synthesized were determined by IR and1H NMR spectra. An X-ray structural analysis of N-chloroacetyl-N′-(4-methylphenylsulfonyl)urea was carried out. It was found that the molecule has the anti-syn conformation stabilized by an intramolecular H-bond. In the crystal, the molecules are combined into centrosymmetrical dimers by intermolecular hydrogen bonds. The compounds considered exhibit moderate fungicide activity. © 1995 Plenum Publishing Corporation. |
|
dc.relation.ispartofseries |
Russian Chemical Bulletin |
|
dc.subject |
arylsulfamides |
|
dc.subject |
biological activity |
|
dc.subject |
chloroacetyl isocyanate |
|
dc.subject |
hydrogen bonds |
|
dc.subject |
N-chloroacetyl-N′-arylsulfonylureas |
|
dc.subject |
X-ray diffraction analysis |
|
dc.title |
Preparation of N-chloroacetyl-N′-arylsulfonylureas and the crystal structure of N-chloroacetyl-N′-(4-methylphenylsulfonyl)urea |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
10 |
|
dc.relation.ispartofseries-volume |
43 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1691 |
|
dc.source.id |
SCOPUS10665285-1994-43-10-SID25444485811 |
|