dc.contributor.author |
Nizamov I. |
|
dc.contributor.author |
Nikitin E. |
|
dc.contributor.author |
Batyeva E. |
|
dc.contributor.author |
Shulaeva M. |
|
dc.contributor.author |
Pozdeev O. |
|
dc.contributor.author |
Cherkasov R. |
|
dc.date.accessioned |
2018-09-18T20:19:12Z |
|
dc.date.available |
2018-09-18T20:19:12Z |
|
dc.date.issued |
2015 |
|
dc.identifier.issn |
1070-4280 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/138674 |
|
dc.description.abstract |
© 2015 Pleiades Publishing, Ltd. Reactions of 4-(1H-pyrrol-1-yl)phenol and 4-(1H-imidazol-1-yl)phenol with 2,4-diaryl-1,3,2λ5,4λ5- dithiadiphosphetane 2,4-disulfides gave the corresponding O-4-hetarylphenyl hydrogen arylphosphonodithioates which were converted into ammonium salts. The latter showed antimicrobial activity against Grampositive bacteria and antifungal activity against fungi of the genus Candida. |
|
dc.relation.ispartofseries |
Russian Journal of Organic Chemistry |
|
dc.title |
Dithiophosphonation of 4-(1H-pyrrol-1-yl)phenol and 4-(1H-imidazol-1-yl)phenol |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
9 |
|
dc.relation.ispartofseries-volume |
51 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1272 |
|
dc.source.id |
SCOPUS10704280-2015-51-9-SID84945250989 |
|