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Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(α-ketoacyl)anthranilic acids Dedicated to Professor Slovenko Polanc on his 65th birthday

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dc.title Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(α-ketoacyl)anthranilic acids Dedicated to Professor Slovenko Polanc on his 65th birthday en
dc.contributor.author Kafka, Stanislav
dc.contributor.author Proisl, Karel
dc.contributor.author Kašpárková, Věra
dc.contributor.author Urankar, Damijana
dc.contributor.author Kimmel, Roman
dc.contributor.author Košmrlj, Janez
dc.relation.ispartof Tetrahedron
dc.identifier.issn 0040-4020 OCLC, Ulrich, Sherpa/RoMEO, JCR
dc.date.issued 2013
utb.relation.volume 69
utb.relation.issue 51
dc.citation.spage 10826
dc.citation.epage 10835
dc.type article
dc.language.iso en
dc.publisher Pergamon en
dc.identifier.doi 10.1016/j.tet.2013.10.092
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0040402013016530
dc.subject N-(α-Ketoacyl)anthranilic acid en
dc.subject Paraperiodic acid en
dc.subject Periodate en
dc.subject Quinolinediones en
dc.subject Quinolinones en
dc.description.abstract N-(α-Ketoacyl)anthranilic acids were prepared by oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones by using paraperiodic acid (H5IO6) or sodium periodate (NaIO4). The optimisation of the reaction conditions is described as well as the utilisation of N-(α-ketoacyl)anthranilic acids in the preparation of anthranilic acid hydrochlorides. © 2013 Elsevier Ltd. All rights reserved. en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1003573
utb.identifier.obdid 43870187
utb.identifier.scopus 2-s2.0-84888639575
utb.identifier.wok 000328808300006
utb.identifier.coden TETRA
utb.source j-scopus
dc.date.accessioned 2013-12-18T16:07:41Z
dc.date.available 2013-12-18T16:07:41Z
utb.contributor.internalauthor Kafka, Stanislav
utb.contributor.internalauthor Proisl, Karel
utb.contributor.internalauthor Kašpárková, Věra
utb.contributor.internalauthor Kimmel, Roman
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