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dc.contributor.author | Nizamov I. | |
dc.contributor.author | Nikitin Y. | |
dc.contributor.author | Belov T. | |
dc.contributor.author | Voloshina A. | |
dc.contributor.author | Batyeva E. | |
dc.contributor.author | Cherkasov R. | |
dc.date.accessioned | 2018-09-19T20:49:02Z | |
dc.date.available | 2018-09-19T20:49:02Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 1042-7163 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/143306 | |
dc.description.abstract | © 2016 Wiley Periodicals, Inc.α-d-Glucofuranose and α-d-allofuranose diacetonides react with 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides to form optically active dithiophosphonates in 78–81% yields, which are transformed into the corresponding ammonium salts in 90–97% yields by the treatment of n-hexadecylamine. The S-silyldithiophosphonate was prepared in 93% yield by the reaction of 2,4-bis(butoxyphenyl) 1,3,2,4-dithiadiphosphetane-2,4-disulfide with silyl ether of α-d-glucofuranose diacetonide. One of the salts obtained possesses antibacterial activity against Staphylococcus aureus ATCC 6538-P. | |
dc.relation.ispartofseries | Heteroatom Chemistry | |
dc.title | α-d-Glucofuranose and α-d-allofuranose diacetonides and silyl ether of α-d-glucofuranose diacetonide in dithiophosphorylation reactions | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 6 | |
dc.relation.ispartofseries-volume | 27 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 345 | |
dc.source.id | SCOPUS10427163-2016-27-6-SID84994086538 |