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.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