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 |
|