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Molecular rearrangement of 9b-hydroxy-imidazo[4,5-c]quinoline-2,4-diones ? a convenient pathway to spiro imidazolidine oxindole derivatives

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dc.title Molecular rearrangement of 9b-hydroxy-imidazo[4,5-c]quinoline-2,4-diones ? a convenient pathway to spiro imidazolidine oxindole derivatives en
dc.contributor.author Klásek, Antonín
dc.contributor.author Mikšík, I.
dc.contributor.author Růžička, A.
dc.contributor.author Lyčka, Antonín
dc.relation.ispartof Helvetica Chimica Acta
dc.identifier.issn 0018-019X Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2009
utb.relation.volume 92
utb.relation.issue 4
dc.citation.spage 689
dc.citation.epage 708
dc.type article
dc.language.iso en
dc.publisher Wiley-VCH Verlag GmbH & Co. en
dc.identifier.doi 10.1002/hlca.200800338
dc.relation.uri http://onlinelibrary.wiley.com/doi/10.1002/hlca.200800338/abstract
dc.subject Rearrangement en
dc.subject Quinolones en
dc.subject Spiro compounds en
dc.subject Mechanism en
dc.subject Isocyanates en
dc.description.abstract 3-Alkyl/Aryl-3-aminochinolin-2,4-diony reagují s isokyanáty na nové titulní sloučeniny. Tyto přesmykují varem v kyselém prostředí a poskytují tři odlišné typy spiro-oxindolů. cs
dc.description.abstract 3-Alkyl/Aryl-3-aminoquinoline-2,4-diones react with isocyanates to give novel title compounds. These compounds rearrange by boiling in acidic environment to give three different type of spiro-oxindoles. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1000990
utb.identifier.rivid RIV/70883521:28110/09:63508076
utb.identifier.obdid 43860112
utb.identifier.scopus 2-s2.0-65549162464
utb.identifier.wok 000265475700010
utb.identifier.coden HCACA
utb.source j-riv
utb.contributor.internalauthor Klásek, Antonín
utb.scopus.affiliation Klásek A., Department of Chemistry, Faculty of Technology, Tomas Bata University, CZ-76272 Zlín, Czech Republic; Lyčka A., Research Institute for Organic Syntheses (VUOS), CZ-53354 Pardubice 20, Rybitví 296, Czech Republic, University of Hradec Králové, Faculty of Education, CZ 50003 Hradec Králové 3, Rokitanského 62, Czech Republic; Mikšǐk I., University of Hradec Králové, Faculty of Education, CZ 50003 Hradec Králové 3, Rokitanského 62, Czech Republic, Institute of Physiology of the Academy of Sciences of the Czech Republic, CZ-14220 Prague, Czech Republic; Růžička A., Department of General and Inorganic Chemistry, Faculty of Chemical Technology, University of Pardubice, CZ-53210 Pardubice, Czech Republic
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