Gold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolones

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dc.contributor.authorDu, Xiaochen
dc.contributor.authorHuang, Jianjun
dc.contributor.authorNechaev, Anton A.
dc.contributor.authorYao, Ruwei
dc.contributor.authorGong, Jing
dc.contributor.authorVan der Eycken, Erik V.
dc.contributor.authorPereshivko, Olga P.
dc.contributor.authorPeshkov, Vsevolod A.
dc.date.accessioned2020-03-31T06:51:12Z
dc.date.available2020-03-31T06:51:12Z
dc.date.issued2018-10-04
dc.description.abstractA series of propargylamides containing an electron-rich benzene ring was prepared through the Ugi reaction of 3,5-dimethoxyaniline with various propiolic acids, aldehydes and isocyanides. Subjecting these adducts to a gold-catalyzed intramolecular alkyne hydroarylation process allowed to efficiently construct the 2-quinolone core bearing a branched substituent on the nitrogen atom...en_US
dc.identifier.citationDu, X.; Huang, J.; Nechaev, A. A.; Yao, R.; Gong, J.; Van der Eycken, E. V.; Pereshivko, O. P.; Peshkov, V. A. Beilstein J. Org. Chem. 2018, 14, 2572–2579. doi:10.3762/bjoc.14.234en_US
dc.identifier.urihttp://nur.nu.edu.kz/handle/123456789/4571
dc.language.isoenen_US
dc.publisherBeilstein J. Org. Chem.en_US
dc.rightsAttribution-NonCommercial-ShareAlike 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/us/*
dc.subjectgold catalysisen_US
dc.subjecthydroarylationen_US
dc.subjectUgi reactionen_US
dc.titleGold-catalyzed post-Ugi alkyne hydroarylation for the synthesis of 2-quinolonesen_US
dc.typeArticleen_US
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