Publikace UTB
Repozitář publikační činnosti UTB

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

Repozitář DSpace/Manakin

Zobrazit minimální záznam


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 OCLC, Ulrich, 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
Find Full text

Soubory tohoto záznamu

Soubory Velikost Formát Zobrazit

K tomuto záznamu nejsou připojeny žádné soubory.

Zobrazit minimální záznam