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 |