An efficient one-pot three-component synthesis of tetrakis(uracil) and their corresponding bis-fused derivatives

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dc.identifier.uri http://dx.doi.org/10.15488/11170
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/11256
dc.contributor.author Abdelmoniem, Amr M. eng
dc.contributor.author Ghozlan, Said A.S. eng
dc.contributor.author Butenschön, Holger eng
dc.contributor.author Abdelmoniem, Doaa M. eng
dc.date.accessioned 2021-08-10T15:25:17Z
dc.date.available 2021-08-10T15:25:17Z
dc.date.issued 2019
dc.identifier.citation Abdelmoniem, A. M.; Ghozlan, S. A. S.; Butenschön, H.; Abdelmoniem, D. M.; Elwahy, A. H. M. et al.: An efficient one-pot three-component synthesis of tetrakis(uracil) and their corresponding bis-fused derivatives. In: Arkivoc 2019 (2019), Nr. 5, S. 163-177. DOI: https://doi.org/10.24820/ark.5550190.p010.875 eng
dc.description.abstract A concise and efficient approach to tetrakis(uracil) derivatives by the reaction of bis(aldehydes) with four equivalents of 6-aminouracil is reported. Also, the synthesis of bis(pyrimido[4,5-b]quinolones) and bis(indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine) derivatives has been accomplished by a three-component reaction involving bis(aldehydes), 6-aminouracil and the appropriate cyclic 1,3-diketone. The method involves domino Knoevenagel condensation / Michael addition reaction sequences. eng
dc.language.iso eng eng
dc.publisher Gainesville : Arkat USA
dc.relation.ispartofseries Arkivoc 2019 (2019), Nr. 5 eng
dc.rights CC BY 4.0 Unported eng
dc.rights.uri https://creativecommons.org/licenses/by/4.0/ eng
dc.subject Bis(aldehydes) eng
dc.subject Michael addition eng
dc.subject uracils eng
dc.subject fused pyrimidines eng
dc.subject quinolinones eng
dc.subject indenones eng
dc.subject.ddc 540 | Chemie eng
dc.title An efficient one-pot three-component synthesis of tetrakis(uracil) and their corresponding bis-fused derivatives eng
dc.type Article eng
dc.type Text eng
dc.relation.essn 1551-7012
dc.relation.doi 10.24820/ark.5550190.p010.875
dc.bibliographicCitation.issue 5
dc.bibliographicCitation.volume 2019
dc.bibliographicCitation.firstPage 163
dc.bibliographicCitation.lastPage 177
dc.description.version publishedVersion eng
tib.accessRights frei zug�nglich eng


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