Please use this identifier to cite or link to this item: 10.3390/M1311
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dc.contributor.authorRucins, Martins-
dc.contributor.authorPajuste, Karlis-
dc.contributor.authorPlotniece, Aiva-
dc.contributor.authorPikun, Nadiia-
dc.contributor.authorRodik, Roman-
dc.contributor.authorVyshnevskiy, Sergiy-
dc.contributor.authorSobolev, Arkadij-
dc.date.accessioned2022-02-01T16:45:01Z-
dc.date.available2022-02-01T16:45:01Z-
dc.date.issued2022-03-
dc.identifier.citationRucins , M , Pajuste , K , Plotniece , A , Pikun , N , Rodik , R , Vyshnevskiy , S & Sobolev , A 2022 , ' Synthesis and characterisation of 1,1'-{[3,5-bis(Dodecyloxy-carbonyl)-4-(thiophen-3-yl)-1,4-dihydropyridine-2,6-diyl]bis-(methylene)}bis(pyridin-1-ium) dibromide ' , MolBank , vol. 2022 , no. 1 , M1311 . https://doi.org/10.3390/M1311-
dc.identifier.issn1422-8599-
dc.identifier.urihttps://dspace.rsu.lv/jspui/handle/123456789/7404-
dc.descriptionFunding Information: Funding: This research was funded by The Joint Ukraine-Latvia R&D Project “Design and study of physicochemical properties and bioactivity of self-assembling calixarene and dihydropyridine hybrids for DNA delivery”, grant number LV-UA/2020/3. Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.description.abstractIn the present work, construction of double-charged cationic amphiphilic 1,1′-{[3,5-bis(dodecyl¬oxy-carbonyl)-4-(thiophen-3-yl)-1,4-dihydropyridine-2,6-diyl]bis-(methylene)}bis(pyridin-1-ium) dibromide (7) was performed in four steps. Dodecyl 3-oxobutanoate (1) was condensed with thiophene-3-carbaldehyde (2) which was necessary for Hantzsch cyclisation dodecyl (E/Z)-3-oxo-2-(thiophen-3-ylmethylene)butanoate (3). Two-component Hantzsch type cyclisation of dodecyl (E/Z)-3-aminobut-2-enoate (4) and dodecyl (E/Z)-3-oxo-2-(thiophen-3-ylmethylene)butanoate (3) gave 3,5-bis(dodecyloxycarbonyl)-2,6-dimethyl-4-(thiophen-3-yl)-1,4-dihydropyridine (5). Bromination of compound 5 followed by nucleophilic substitution of bromine with pyridine gave the desired cationic amphiphilic 1,4-dihydropyridine 7. The obtained target compound 7 and new intermediates 3, 5 and 6 were fully characterised by IR, UV,1 H NMR,13 C NMR, HRMS or microanalysis. Characterisation of nanoparticles formed by the cationic 1,4-dihydropyridine 7 in an aqueous solution was performed by DLS measurements.en
dc.format.extent401403-
dc.language.isoeng-
dc.relation.ispartofMolBank-
dc.rightsinfo:eu-repo/semantics/openAccess-
dc.subject1,4-dihydropyridines-
dc.subjectDLS-
dc.subjectNanoparticles-
dc.subjectSelf-assembling properties-
dc.subjectSynthetic lipids-
dc.subject1.4 Chemical sciences-
dc.subject1.6 Biological sciences-
dc.subject1.1. Scientific article indexed in Web of Science and/or Scopus database-
dc.subjectBiochemistry-
dc.subjectPhysical and Theoretical Chemistry-
dc.subjectOrganic Chemistry-
dc.titleSynthesis and characterisation of 1,1'-{[3,5-bis(Dodecyloxy-carbonyl)-4-(thiophen-3-yl)-1,4-dihydropyridine-2,6-diyl]bis-(methylene)}bis(pyridin-1-ium) dibromideen
dc.type/dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article-
dc.identifier.doi10.3390/M1311-
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85121780495&partnerID=8YFLogxK-
dc.description.statusPeer reviewed-
Appears in Collections:Research outputs from Pure / Zinātniskās darbības rezultāti no ZDIS Pure

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