Efficient synthesis of novel bis(dihydropyrano[2,3c]pyrazoles), bis(4H-chromenes) and bis(dihydropyrano[3,2-c]chromenes) with amide functionality

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dc.identifier.uri http://dx.doi.org/10.15488/10770
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/10848
dc.contributor.author Abdella, Amna M. eng
dc.contributor.author Abdelmoniem, Amr M. eng
dc.contributor.author Butenschön, Holger eng
dc.contributor.author Abdelhamid, Ismail A. eng
dc.contributor.author Elwahy, Ahmed H.M. eng
dc.date.accessioned 2021-04-20T15:29:15Z
dc.date.available 2021-04-20T15:29:15Z
dc.date.issued 2019
dc.identifier.citation Abdella, A.M.; Abdelmoniem, A.M.; Butenschön, H.; Abdelhamid, I.A.; Elwahy, A.H.M.: Efficient synthesis of novel bis(dihydropyrano[2,3c]pyrazoles), bis(4H-chromenes) and bis(dihydropyrano[3,2-c]chromenes) with amide functionality. In: Arkivoc 4 (2019), S. 306-324. DOI: https://doi.org/10.24820/ark.5550190.p011.071 eng
dc.description.abstract A synthesis of novel bis(1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitriles), bis(4H-chromene-3-carbonitriles) and bis(dihydropyrano[3,2-c]chromenes), which are linked to aliphatic spacers via amide linkages was achieved via multicomponent reactions (MCR) of the appropriate bis-aldehyde with two equivalents of both of malononitrile and 3-methylpyrazol-5-one, dimedone or 4-hydroxycoumarin in a basic solution. eng
dc.language.iso eng eng
dc.publisher Zürich : ARKAT
dc.relation.ispartofseries Arkivoc 4 (2019) eng
dc.rights CC BY 4.0 Unported eng
dc.rights.uri https://creativecommons.org/licenses/by/4.0/ eng
dc.subject Bis(pyrano[2,3-c]pyrazole) eng
dc.subject bis(chromene) eng
dc.subject bis(pyrano[3,2-c]chromene) eng
dc.subject amide linkages eng
dc.subject.ddc 540 | Chemie eng
dc.title Efficient synthesis of novel bis(dihydropyrano[2,3c]pyrazoles), bis(4H-chromenes) and bis(dihydropyrano[3,2-c]chromenes) with amide functionality eng
dc.type Article eng
dc.type Text eng
dc.relation.essn 1551-7012
dc.relation.issn 1551-7004
dc.relation.doi 10.24820/ark.5550190.p011.071
dc.bibliographicCitation.firstPage 306
dc.bibliographicCitation.lastPage 324
dc.description.version publishedVersion eng
tib.accessRights frei zug�nglich eng


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