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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 |