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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 |