New approach to N,N-dialkoxy-N'-arylureas and N,N-dialkoxycarbamates

Please use this identifier to cite or link to this item: https://dspace.usfa.edu.ua/handle/123456789/1114

Title:	New approach to N,N-dialkoxy-N'-arylureas and N,N-dialkoxycarbamates
Authors:	Shtamburg, Vasiliy G. Tsygankov, Alexander V. Gerasimenko, Mikhail V. Shishkin, Oleg V. Zubatyuk, Roman I. Mazepa, Alexander V. Kostyanovsky, Remir G.
Keywords:	N-ACYLNITRENIUM IONS ELECTROPHILIC AROMATIC-SUBSTITUTION GEMINAL SYSTEMS N,N-DIALKOXYUREAS NITROGEN METHOXYAMIDES ALKOXYAMIDES ALKOXYUREAS ALCOHOLYSIS
Issue Date:	2011
Publisher:	ELSEVIER SCIENCE BV, PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
Citation:	New 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.2011.01.021
Abstract:	Methanolysis 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.
URI:	http://dspace.sfa.org.ua:80/handle/123456789/1114
Appears in Collections:	Наукові публікації

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