Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12578
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dc.rights.licenserestrictedAccess-
dc.contributor.authorMilović E.-
dc.contributor.authorJanković, Nenad-
dc.contributor.authorVranes, Milan-
dc.contributor.authorStefanovic D.-
dc.contributor.authorPetronijević, Jelena-
dc.contributor.authorJoksimović N.-
dc.contributor.authorMuškinja, Jovana-
dc.contributor.authorRatković, Zoran-
dc.date.accessioned2021-04-20T21:11:47Z-
dc.date.available2021-04-20T21:11:47Z-
dc.date.issued2021-
dc.identifier.issn1610-3653-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/12578-
dc.description.abstract© 2020, Springer Nature Switzerland AG. Reactions in water as a safe and cheap solvent is a major goal of green chemistry. Actual synthesis of pyrido-dipyrimidine scaffold, named DNA-base hybrids, involves catalysis in hazardous solvents. Here we synthesised pyrido-dipyrimidines by one-pot heterocyclization of thiobarbituric acid, vanillic aldehydes and amines in water. Enamine and vanillidene are key intermediates of the Biginelli-like reaction mechanism. Our synthetic method displays several benefits such as the use of a green medium and various substrates, and yields up to 99%.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceEnvironmental Chemistry Letters-
dc.titleGreen one-pot synthesis of pyrido-dipyrimidine DNA-base hybrids in water-
dc.typearticle-
dc.identifier.doi10.1007/s10311-020-01076-9-
dc.identifier.scopus2-s2.0-85089546020-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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