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 |
|