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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
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