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dc.contributor.author | Nizamov I. | |
dc.contributor.author | Terenzhev D. | |
dc.contributor.author | Shumatbaev G. | |
dc.contributor.author | Batyeva E. | |
dc.contributor.author | Cherkasov R. | |
dc.date.accessioned | 2018-09-19T21:00:24Z | |
dc.date.available | 2018-09-19T21:00:24Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 1070-3632 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/143501 | |
dc.description.abstract | © 2016, Pleiades Publishing, Ltd.Carvacrol trimethylsilyl ether when reacting with P4S10 forms S-trimethylsilyl ester of O,O-bis(5-isopropyl-2-methylphenyl)dithiophosphoric acid. The reactions of 2,4-diorganyl-1,3,2,4-dithiadiphosphetane-2,4-disulfides with carvacrol (thymol) trimethylsilyl ether yield the S-trimethylsilyl esters of the corresponding dithiophosphoric acids. | |
dc.relation.ispartofseries | Russian Journal of General Chemistry | |
dc.subject | carvacrol | |
dc.subject | dithiophosphate | |
dc.subject | dithiophosphonate | |
dc.subject | dithiophosphorylation | |
dc.subject | phosphorus sulfide | |
dc.subject | silyl ether | |
dc.subject | thymol | |
dc.title | Dithiophosphorylation of trimethylsilyl ethers of carvacrol and thymol | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 3 | |
dc.relation.ispartofseries-volume | 86 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 564 | |
dc.source.id | SCOPUS10703632-2016-86-3-SID84969593697 |