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Completely dissimilar: The reactivity of 1-unsubstituted 3-chloroquinoline-2,4-diones with ethylene diamine and ethanolamine to form new molecular rearrangements

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dc.title Completely dissimilar: The reactivity of 1-unsubstituted 3-chloroquinoline-2,4-diones with ethylene diamine and ethanolamine to form new molecular rearrangements en
dc.contributor.author Klásek, Antonín
dc.contributor.author Lyčka, Antonín
dc.contributor.author Rouchal, Michal
dc.relation.ispartof Arkivoc
dc.identifier.issn 1551-7004 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2020
utb.relation.volume 2020
utb.relation.issue 6
dc.citation.spage 209
dc.citation.epage 219
dc.type article
dc.language.iso en
dc.publisher Arkat
dc.identifier.doi 10.24820/ARK.5550190.P011.053dummy2
dc.relation.uri https://www.arkat-usa.org/get-file/69213/
dc.subject α-Aminoketones en
dc.subject indolones en
dc.subject quinazolinones en
dc.subject quinolinediones en
dc.subject rearrangement en
dc.description.abstract 3-Chloroquinoline-2,4-diones react with ethanolamine to give 3-hydroxyethylaminoquinoline-2,4-diones. By reacting with isothiocyanic acid, these compounds cyclize to form thioxoimidazo derivatives. If a benzyl group is attached to carbon atom C-3, it is cleaved off. Simultaneously, molecular rearrangement proceeds through the formation of compounds with quinazoline skeletons. However, when using ethylene diamine, the compounds are subject to new types of molecular rearrangement leading to the formation of new quinazoline derivatives. © AUTHOR(S) en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1009876
utb.identifier.obdid 43881662
utb.identifier.scopus 2-s2.0-85090146812
utb.identifier.wok 000584517600019
utb.identifier.coden AGFUA
utb.source j-scopus
dc.date.accessioned 2020-09-15T13:41:16Z
dc.date.available 2020-09-15T13:41:16Z
dc.description.sponsorship TBU in Zlin [IGA/FT/2019/010]
dc.rights Attribution 4.0 International
dc.rights.uri http://creativecommons.org/licenses/by/4.0/
dc.rights.access openAccess
utb.ou Department of Chemistry
utb.contributor.internalauthor Klásek, Antonín
utb.contributor.internalauthor Rouchal, Michal
utb.fulltext.affiliation Antonin Klásek a*, Antonin Lyčka b, Michal Rouchal a a Department of Chemistry, Faculty of Technology, Tomas Bata University, CZ-762 72 Zlín, Czech Republic b University of Hradec Králové, Faculty of Science, Rokitanského 62, CZ-500 03 Hradec Králové 3, Czech Republic E-mail: klasek@utb.cz
utb.fulltext.dates -
utb.fulltext.sponsorship A.K. and M.R. grateful for the financial support from the internal grant of TBU in Zlin No. IGA/FT/2019/010, funded from the resources of specific university research. The authors would also like to thank Mrs. H. Geržová (Faculty of Technology, Tomas Bata University in Zlín) for her technical assistance.
utb.wos.affiliation [Klasek, Antonin; Rouchal, Michal] Tomas Bata Univ, Fac Technol, Dept Chem, CZ-76272 Zlin, Czech Republic; [Lycka, Antonin] Univ Hradec Kralove, Fac Sci, Rokitanskeho 62, CZ-50003 Hradec Kralove 3, Czech Republic
utb.scopus.affiliation Department of Chemistry, Faculty of Technology, Tomas Bata University, Zlín, CZ-762 72, Czech Republic; University of Hradec Králové, Faculty of Science, Rokitanského 62, Hradec Králové 3, CZ-500 03, Czech Republic
utb.fulltext.projects IGA/FT/2019/010
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