Please use this identifier to cite or link to this item: http://hdl.handle.net/11701/16709
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dc.contributor.authorSakharov, Pavel A.-
dc.contributor.authorKoronatov, Alexander N.-
dc.contributor.authorKhlebnikov, Alexander F.-
dc.contributor.authorNovikov, Mikhail S.-
dc.contributor.authorGlukharev, Artem G.-
dc.contributor.authorRogacheva, Elizaveta V.-
dc.contributor.authorKraeva, Liudmila A.-
dc.contributor.authorSharoyko, Vladimir V.-
dc.contributor.authorTennikova, Tatiana B.-
dc.contributor.authorRostovskii, Nikolai V.-
dc.date.accessioned2019-11-28T13:16:04Z-
dc.date.available2019-11-28T13:16:04Z-
dc.date.issued2019-11-21-
dc.identifier.citationRSC Adv., 2019, 9, 37901en_GB
dc.identifier.urihttp://hdl.handle.net/11701/16709-
dc.description.abstractNon-natural 2H-azirine-2-carboxylic acids were obtained in high yields by FeCl2-catalyzed isomerization of 5-chloroisoxazoles to azirine-2-carbonyl chlorides followed by their hydrolysis. The 3-aryl- and 3- heteroaryl-substituted acids are stable during prolonged storage, exhibit antibacterial activity against ESKAPE pathogens and show a low level of cytotoxicityen_GB
dc.description.sponsorshipthe Scientifc Council of the President of the Russian Federation (MK-2698.2019.3)en_GB
dc.language.isoenen_GB
dc.publisherThe Royal Society of Chemistryen_GB
dc.relation.ispartofseries10.1039/c9ra09345a;-
dc.titleNon-natural 2H-azirine-2-carboxylic acids: an expedient synthesis and antimicrobial activityen_GB
dc.typeArticleen_GB
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