dc.contributor.author |
Antipin I. |
|
dc.contributor.author |
Stoikov I. |
|
dc.contributor.author |
Khrustalev A. |
|
dc.contributor.author |
Konovalov A. |
|
dc.date.accessioned |
2018-09-17T21:17:33Z |
|
dc.date.available |
2018-09-17T21:17:33Z |
|
dc.date.issued |
2001 |
|
dc.identifier.issn |
1066-5285 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/134794 |
|
dc.description.abstract |
A new type of macrocyclic receptor able to bind organic substrates containing carboxy and carboxylate groups was designed on the basis of 1,3-disubstituted calix[4]arenes. A series of disubstitited calix[4]arenes were prepared in 60-80% yields by selective 1,3-alkylation of p-tert-butylcalix[4]arene. The compounds obtained were tested as carriers for DL-tartaric, glycolic, DL-amygdalic, and DL-glutamic acids through liquid membranes immobilized on a polymer matrix. The structural factors favorable for the transport of these hydrophilic substrates through lipophilic membranes were established. |
|
dc.relation.ispartofseries |
Russian Chemical Bulletin |
|
dc.subject |
α-amino acids |
|
dc.subject |
α-hydroxy acids |
|
dc.subject |
Alkylation |
|
dc.subject |
Calix[4]arene |
|
dc.subject |
Membrane transport |
|
dc.title |
Membrane extraction of organic compounds 3. A new receptor fragment for carboxylate groups based of the calix[4]arene platform |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
11 |
|
dc.relation.ispartofseries-volume |
50 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
2134 |
|
dc.source.id |
SCOPUS10665285-2001-50-11-SID0035541786 |
|