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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2011 Volume 21, Issue 1, Pages 50–52 (Mi mendc2864)

This article is cited in 16 papers

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

V. G. Shtamburga, A. V. Tsygankovb, M. V. Gerasimenkoa, O. V. Shishkincd, R. I. Zubatyukc, A. V. Mazepae, R. G. Kostyanovskyf

a Ukrainian State University of Chemical Technology, Dnepropetrovsk, Ukraine
b State Flight Academy of Ukraine, Kirovograd, Ukraine
c STC 'Institute for Single Crystals', National Academy of Sciences of Ukraine, Kharkov, Ukraine
d Department of Chemistry, V.N. Karazin Khar'kov National University, Khar'kov, Ukraine
e A.V. Bogatsky Physico-Chemical Institute, National Academy of Sciences of Ukraine, Odessa, Ukraine
f N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Methanolysis of N-chloro-N-alkoxy-N’-arylureas in the presence of silver trifluoroacetate gives the corresponding N,N-dialkoxy-N’-arylureas, whereas N-chloro-N-alkoxycarbamates react with alcohols in the presence of silver trifluoroacetate to afford N,N-dialkoxycarbamates.

Language: English

DOI: 10.1016/j.mencom.2011.01.021



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