Показать сокращенную информацию
dc.contributor.author | Nizamov I. | |
dc.contributor.author | Terenzhev D. | |
dc.contributor.author | Ivshin K. | |
dc.contributor.author | Kataeva O. | |
dc.contributor.author | Shulaeva M. | |
dc.contributor.author | Pozdeev O. | |
dc.contributor.author | Batyeva E. | |
dc.contributor.author | Cherkasov R. | |
dc.date.accessioned | 2019-01-22T20:36:17Z | |
dc.date.available | 2019-01-22T20:36:17Z | |
dc.date.issued | 2018 | |
dc.identifier.issn | 0268-2605 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/147929 | |
dc.description.abstract | Copyright © 2018 John Wiley & Sons, Ltd. Chiral S-tributylstannyl dithiophosphates and dithiophosphonates were obtained by the reactions of optically active dithiophosphoric and dithiophosphonic acids containing (S)-(–)-menthyl and (R)-(+)-menthyl substituents with gaseous ammonia and tributyl chlorostannane. The reactions of chiral ammonium dithiophosphate containing (1R)-endo-(+)-fenchyl substituent with tributyl chlorostannane or tetrachlorostannane result in corresponding S-tributylstannyl dithiophosphate or tetrakis(dithiophosphato)stannane. Molecular structure of ammonium O,O-di-(–)-menthyldithiophosphate was studied by X-ray single crystal diffraction. Bactericidal activity of S-tributylstannyl dithiophosphates was tested. | |
dc.relation.ispartofseries | Applied Organometallic Chemistry | |
dc.subject | bactericidal activity | |
dc.subject | dithiophosphates | |
dc.subject | dithiophosphonates | |
dc.subject | monoterpenyl alcohols | |
dc.subject | stannyl derivatives | |
dc.title | Chiral S-stannyl dithiophosphates and dithiophosphonates on the basis of monoterpenols | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 5 | |
dc.relation.ispartofseries-volume | 32 | |
dc.collection | Публикации сотрудников КФУ | |
dc.source.id | SCOPUS02682605-2018-32-5-SID85043384366 |