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dc.contributor.author | Kolodyazhnaya O. | |
dc.contributor.author | Kolodyazhnyi O. | |
dc.contributor.author | Cherkasov R. | |
dc.contributor.author | Garifzyanov A. | |
dc.contributor.author | Davletshina N. | |
dc.contributor.author | Koshkin S. | |
dc.date.accessioned | 2018-09-18T20:18:47Z | |
dc.date.available | 2018-09-18T20:18:47Z | |
dc.date.issued | 2014 | |
dc.identifier.issn | 1070-3632 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/138602 | |
dc.description.abstract | Bisphosphonates derived from natural terpenes were synthesized by phosphonylation of corresponding aldehydes. The general strategy of introduction of the phosphonate groups into the polyprenol molecule involves successive treatment of a hydroxyl compound by Swern reagent to oxidize the C-OH group into C=O and a (EtO)3P/[PyH]+ClO - 4 mixture to phosphylate the resulting carbonyl compound. © 2014 Pleiades Publishing, Ltd. | |
dc.relation.ispartofseries | Russian Journal of General Chemistry | |
dc.subject | bisphosphonates | |
dc.subject | hydrophosphonates | |
dc.subject | phosphonylation | |
dc.subject | pyridinium perchlorate | |
dc.subject | terpene derivatives | |
dc.title | Synthesis of α-hydroxy(polyprenyl) bisphosphonates | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 4 | |
dc.relation.ispartofseries-volume | 84 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 647 | |
dc.source.id | SCOPUS10703632-2014-84-4-SID84901032592 |