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Enantioselective recognition of amino acids by enantiomerically pure calix[4]arene carboxylic acid or their diastereomerically pure N-(1-phenyl)ethyl amides

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dc.contributor.author Andreyko E.
dc.contributor.author Stoikov I.
dc.contributor.author Antipin I.
dc.contributor.author Karpus A.
dc.contributor.author Sikorsky A.
dc.contributor.author Yesypenko O.
dc.contributor.author Rozhenko A.
dc.contributor.author Boyko V.
dc.contributor.author Kalchenko V.
dc.date.accessioned 2018-09-18T20:35:01Z
dc.date.available 2018-09-18T20:35:01Z
dc.date.issued 2013
dc.identifier.issn 1998-9539
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/141380
dc.description.abstract The interaction of inherently chiral calix[4]arene carboxilic acids and their amides with amino acids in the organic phase has been studied using electron spectroscopy. It was found that the chiral calix[4]arenes are able of enantioselective recognition of L- and D-forms of amino acids. Stability constants of the calixarene - amino acid supramolecular complexes were determined and mechanism of the host-guest interaction was examined by molecular modeling method. © ISUCT Publishing.
dc.relation.ispartofseries Macroheterocycles
dc.subject Chiral calix[4]arenes
dc.subject DFT
dc.subject Electron spectroscopy
dc.subject Enantioselective recognition
dc.title Enantioselective recognition of amino acids by enantiomerically pure calix[4]arene carboxylic acid or their diastereomerically pure N-(1-phenyl)ethyl amides
dc.type Article
dc.relation.ispartofseries-issue 3
dc.relation.ispartofseries-volume 6
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 227
dc.source.id SCOPUS19989539-2013-6-3-SID84923513450


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  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

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