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

Klásek, Antonín; Mikšík, I.; Růžička, A.; Lyčka, Antonín

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