Please use this identifier to cite or link to this item: http://dspace.sfa.org.ua:80/handle/123456789/1115
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dc.contributor.authorShtamburg, Vasiliy G.-
dc.contributor.authorTsygankov, Alexander V.-
dc.contributor.authorShishkin, Oleg V.-
dc.contributor.authorZubatyuk, Roman I.-
dc.contributor.authorUspensky, Boris V.-
dc.contributor.authorShtamburg, Victor V.-
dc.contributor.authorVictor V., Alexander V.-
dc.contributor.authorKostyanovsky, Remir G.-
dc.date.accessioned2021-04-20T08:03:22Z-
dc.date.available2021-04-20T08:03:22Z-
dc.date.issued2012-
dc.identifier.citationThe properties and structure of N-chloro-N-methoxy-4-nitrobenzamide / Vasiliy G. Shtamburg, Alexander V. Tsygankov, Oleg V. Shishkin and others // Mendeleev Commun. - 2012. - Volume: 22; Issue: 3. - P. 164-166. DOI: 10.1016/j.mencom.2012.05.019en_US
dc.identifier.urihttp://dspace.sfa.org.ua:80/handle/123456789/1115-
dc.description.abstractThe XRD study of N-chloro-N-methoxy-4-nitrobenzamide revealed the high pyramidality degree of its amide nitrogen atom in O–N–Cl moiety. N-Chloro-N-methoxy-4-nitrobenzamide reacts with AcONa in MeCN selectively forming N-acetoxy-N-methoxy-4-nitrobenzamide, whereas its methanolysis in the presence of AcONa yields N,N'-bis(4-nitrobenzoyl)-N,N'-dimethoxyhydrazine.en_US
dc.language.isoenen_US
dc.publisherELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSen_US
dc.subjectACYLOXY-N-ALKOXYAMIDESen_US
dc.subjectGEMINAL SYSTEMSen_US
dc.subjectCRYSTAL-STRUCTURESen_US
dc.subjectANOMERIC AMIDESen_US
dc.subjectNITROGENen_US
dc.subjectALKOXYUREASen_US
dc.subjectDERIVATIVESen_US
dc.subjectUREASen_US
dc.titleThe properties and structure of N-chloro-N-methoxy-4-nitrobenzamideen_US
dc.typeArticleen_US
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