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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 |