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dc.contributor.author | Cherkasov R. | |
dc.contributor.author | Galkin V. | |
dc.contributor.author | Khusainova N. | |
dc.contributor.author | Mostovaya O. | |
dc.contributor.author | Garifzyanov A. | |
dc.contributor.author | Nuriazdanova G. | |
dc.contributor.author | Krasnova N. | |
dc.contributor.author | Berdnikov E. | |
dc.date.accessioned | 2018-09-17T21:28:07Z | |
dc.date.available | 2018-09-17T21:28:07Z | |
dc.date.issued | 2005 | |
dc.identifier.issn | 1070-4280 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/135036 | |
dc.description.abstract | New and previously known β-aminoethylphosphonates were synthesized by addition of primary and secondary amines to vinylphosphonates, and their IR and NMR spectra were examined. Diethyl 2-diethyl-aminoethylphosphonate and diethyl 2-morpholinoethylphosphonate were found to be stronger bases than the corresponding aminomethylphosphonates, but all these are weaker bases than their precursors, nonphosphorylated amines. Distribution constants of β-aminophosphonates between water and some organic solvents were determined and compared with those of their α-amino homologs. © 2005 Pleiades Publishing, Inc. | |
dc.relation.ispartofseries | Russian Journal of Organic Chemistry | |
dc.title | Synthesis of β-aminophosphonates and study of their acid-base properties and phase distribution in water-organic solvent systems | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 10 | |
dc.relation.ispartofseries-volume | 41 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 1481 | |
dc.source.id | SCOPUS10704280-2005-41-10-SID29244489542 |