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p-tert-butyl thiacalix[4]arene derivatives functionalized in the lower rim with bis(3-aminopropyl)amine: Synthesis and interaction with DNA

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dc.contributor.author Puplampu J.
dc.contributor.author Yakimova L.
dc.contributor.author Vavilova A.
dc.contributor.author Rizvanov I.
dc.contributor.author Stoikov I.
dc.date.accessioned 2018-09-18T20:35:07Z
dc.date.available 2018-09-18T20:35:07Z
dc.date.issued 2015
dc.identifier.issn 1998-9539
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/141388
dc.description.abstract © ISUCT Publishing. New tetrasubstituted derivatives of thiacalix[4]arene functionalized with bis(3-aminopropyl)amide fragments at the lower rim in the cone and 1,3-alternate conformations have been synthesized. It was demonstrated that the synthesized thiacalix[4]arenes derivatives interact with DNA resulting in a shift in absorption maxima to 257 nm with clear isosbestic point at 300 nm.
dc.relation.ispartofseries Macroheterocycles
dc.subject DNA
dc.subject Macrocycles
dc.subject Molecular recognition
dc.subject Synthesis
dc.subject Thiacalix[4]arene
dc.title p-tert-butyl thiacalix[4]arene derivatives functionalized in the lower rim with bis(3-aminopropyl)amine: Synthesis and interaction with DNA
dc.type Article
dc.relation.ispartofseries-issue 1
dc.relation.ispartofseries-volume 8
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 75
dc.source.id SCOPUS19989539-2015-8-1-SID84932633348


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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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