Thermal rearrangement of 3-hydroxy-1H,3H-quinoline-2,4-diones to 3-acyloxy-2,3-dihydro-1H-indol-2-ones

Klásek, Antonín; Kořistek, Kamil; Kafka, Stanislav; Košmrlj, Janez

dc.title	Thermal rearrangement of 3-hydroxy-1H,3H-quinoline-2,4-diones to 3-acyloxy-2,3-dihydro-1H-indol-2-ones	en
dc.contributor.author	Klásek, Antonín
dc.contributor.author	Kořistek, Kamil
dc.contributor.author	Kafka, Stanislav
dc.contributor.author	Košmrlj, Janez
dc.relation.ispartof	Heterocycles
dc.identifier.issn	0385-5414 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued	2003
utb.relation.volume	60
utb.relation.issue	8
dc.citation.spage	1811
dc.citation.epage	1820
dc.type	article
dc.language.iso	en
dc.publisher	Japan Institute of Heterocyclic Chemistry Publication	en
dc.identifier.doi	10.3987/COM-03-9796
dc.subject	molekulární přesmyk	cs
dc.subject	indolony	cs
dc.subject	chinolindiony	cs
dc.subject	molecular rearrangement	en
dc.subject	indolones	en
dc.subject	quinolinediones	en
dc.description.abstract	3-Alkyl/aryl-3-hydroxy-1H,3H-quinoline-2,4-diones (2) were transformed into isomeric 3-acyloxy-2,3-dihydro-1H-indol-2-ones (3) by thermally induced molecular rearrangement. All products were characterized by their 1H NMR, 13C NMR, and IR spectra.	en
utb.faculty	Faculty of Technology
dc.identifier.uri	http://hdl.handle.net/10563/1000237
utb.identifier.rivid	RIV/70883521:28110/03:63501405
utb.identifier.obdid	11552917
utb.identifier.scopus	2-s2.0-0042467888
utb.identifier.wok	000184978500005
utb.source	j-riv
utb.contributor.internalauthor	Klásek, Antonín
utb.contributor.internalauthor	Kořistek, Kamil
utb.contributor.internalauthor	Kafka, Stanislav