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 |
|