Geminal systems 64.*N-Alkoxy-N-chloroureas and N,N-dialkoxyureas

dc.contributor.authorShtamburg, V. G.en
dc.contributor.authorKostyanovsky, R. G.en
dc.contributor.authorTsygankov, A. V.en
dc.contributor.authorShtamburg, V. V.en
dc.contributor.authorShishkin, O. V.en
dc.contributor.authorZubatyuk, R. I.en
dc.contributor.authorMazepa, A. V.en
dc.contributor.authorKravchenko, S. V.en
dc.date.accessioned2018-06-26T09:49:02Z
dc.date.available2018-06-26T09:49:02Z
dc.date.issued2015
dc.description.abstractMolecular and crystal structures of N-alkoxy-N-chloroureas and N,N-dialkoxyureas were studied together with those of N-alkoxyureas as reference compounds. N-Alkoxy-N-chloroureas were found to have an elongated N—Cl bond and a shortened N—O(Alk) bond due to the nO(Alk)*N—Cl anomeric effect. Alcoholysis of N-alkoxy-N-chloro derivatives of urea, N´-arylureas, and carbamates in the presence of silver trifluoroacetate leads to sterically hindered N,N-dialkoxyureas, N,N-dialkoxy-N´-arylureas, and N,N-dialkoxycarbamates, respectively.en
dc.identifier.citationGeminal systems 64.*N-Alkoxy-N-chloroureas and N,N-dialkoxyureas / V. G. Shtamburg [et al.] // Russian Chemical Bulletin. – 2015. – Vol.64, № 1. – P. 62-75.en
dc.identifier.urihttps://repository.kpi.kharkov.ua/handle/KhPI-Press/36916
dc.language.isoen
dc.publisherSpringer and Business Media, Inc.en
dc.subjectN-alkoxy-N-chloroureasen
dc.subjectanomeric effecten
dc.subjectN-acyloxy-N-alkoxyureasen
dc.subjectN-alkoxy-N-chlorocarbamatesen
dc.subjectalcoholysisen
dc.subjectureasen
dc.subjectcarbamatesen
dc.titleGeminal systems 64.*N-Alkoxy-N-chloroureas and N,N-dialkoxyureasen
dc.typeArticleen

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