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dc.contributor.authorShtamburg, Vasiliy G.-
dc.contributor.authorTsygankov, Alexander V.-
dc.contributor.authorGerasimenko, Mikhail V.-
dc.contributor.authorShishkin, Oleg V.-
dc.contributor.authorZubatyuk, Roman I.-
dc.contributor.authorMazepa, Alexander V.-
dc.contributor.authorKostyanovsky, Remir G.-
dc.date.accessioned2021-04-16T09:30:39Z-
dc.date.available2021-04-16T09:30:39Z-
dc.date.issued2011-
dc.identifier.citationNew approach to N,N-dialkoxy-N'-arylureas and N,N-dialkoxycarbamates / Vasiliy G. Shtamburg, Alexander V. Tsygankov, Mikhail V. Gerasimenko and others // Mendeleev Commun. - 2011. - Volume: 21; Issue: 1. - P. 50-52. DOI: 10.1016/j.mencom.2011.01.021en_US
dc.identifier.urihttp://dspace.sfa.org.ua:80/handle/123456789/1114-
dc.description.abstractMethanolysis of N-chloro-N-alkoxy-N'-arylureas in the presence of silver trifluoroacetate gives the corresponding N,N-dialkoxyN'-arylureas, whereas N-chloro-N-alkoxycarbamates react with alcohols in the presence of silver trifluoroacetate to afford N,N-dialkoxy carbamates.en_US
dc.publisherELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSen_US
dc.subjectN-ACYLNITRENIUM IONSen_US
dc.subjectELECTROPHILIC AROMATIC-SUBSTITUTIONen_US
dc.subjectGEMINAL SYSTEMSen_US
dc.subjectN,N-DIALKOXYUREASen_US
dc.subjectNITROGENen_US
dc.subjectMETHOXYAMIDESen_US
dc.subjectALKOXYAMIDESen_US
dc.subjectALKOXYUREASen_US
dc.subjectALCOHOLYSISen_US
dc.titleNew approach to N,N-dialkoxy-N'-arylureas and N,N-dialkoxycarbamatesen_US
dc.typeArticleen_US
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