dc.contributor.author |
Nizamov I. |
|
dc.contributor.author |
Yambushev F. |
|
dc.contributor.author |
Voloshina A. |
|
dc.contributor.author |
Alfonsov V. |
|
dc.date.accessioned |
2018-09-18T20:13:54Z |
|
dc.date.available |
2018-09-18T20:13:54Z |
|
dc.date.issued |
2013 |
|
dc.identifier.issn |
1042-7163 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/137779 |
|
dc.description.abstract |
The Kabachnik-Fields reaction of E,Z-citral with diethyl phosphite in the presence of isobutylamine has been found to form α-aminophosphonates. The Pudovik reactions of diethyl phosphite with prenyl imines prepared on the basis of E,Z-citral with isobutylamine also allowed us to obtain the same α-aminophosphonates. We have managed to synthesize α- aminophosphonates by the reaction of O,O-dialkyl trimethylsilyl phosphites with prenyl imines in the presence of water or diethylamine. α- Aminophosphonates were also synthesized by the reaction of diethyl phosphite with (R,S)-citronellal in the presence of alkylamines. α-Aminophosphonates obtained showed bacteriostatic activity against Staphylococcus aureus and Bacillus cereus. © 2012 Wiley Periodicals, Inc. |
|
dc.relation.ispartofseries |
Heteroatom Chemistry |
|
dc.title |
The kabachnik-fields and pudovik reactions on the basis of E,Z-citral and its imines and (R,S)-citronellal |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
1 |
|
dc.relation.ispartofseries-volume |
24 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
36 |
|
dc.source.id |
SCOPUS10427163-2013-24-1-SID84872268524 |
|