dc.contributor.author |
Nizamov I. |
|
dc.contributor.author |
Terenzhev D. |
|
dc.contributor.author |
Shumatbaev G. |
|
dc.contributor.author |
Islamov D. |
|
dc.contributor.author |
Kataeva O. |
|
dc.contributor.author |
Cherkasov R. |
|
dc.date.accessioned |
2018-09-19T20:48:12Z |
|
dc.date.available |
2018-09-19T20:48:12Z |
|
dc.date.issued |
2016 |
|
dc.identifier.issn |
1042-6507 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/143279 |
|
dc.description.abstract |
© 2016 Taylor & Francis Group, LLC.Novel 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfideswere prepared by the reactions of tetraphosphorus decasulfide with butylphenyl ether or 3-brominephenyl-1-isoamyl ether in 1,2-dichlorobenzene. Their structures were established by X-ray single crystal diffraction. Chiral S-trimethylsilyl dithiophosphonates were prepared by the reactions of 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides with trimethyl silyl ethers of monoterpenols. Unsaturated S-trimethylsilyl dithiophosphonates were synthesized by the reactions of 2,4-diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides with O-trimethylsilyl ethers of geraniol, nerol, and (R,S)-linalool. S-Esters of dithiophosphonic acids, which possessed antimicrobial activity, were prepared by the reactions of chiral S-trimethylsilyl dithiophosphonateswith orthoformiates, acetals and thioacetals. |
|
dc.relation.ispartofseries |
Phosphorus, Sulfur and Silicon and the Related Elements |
|
dc.subject |
1,3,2,4-Dithiadiphosphetane-2,4-disulfides |
|
dc.subject |
dithiophosphorylation |
|
dc.subject |
monoterpenols |
|
dc.subject |
silylation |
|
dc.title |
2,4-Diorganyl 1,3,2,4-dithiadiphosphetane-2,4-disulfides, their structure and S-silyl dithiophosphonic derivatives |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
11-12 |
|
dc.relation.ispartofseries-volume |
191 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
1576 |
|
dc.source.id |
SCOPUS10426507-2016-191-1112-SID84992578616 |
|