Geminal systems 64.*N-Alkoxy-N-chloroureas and N,N-dialkoxyureas
dc.contributor.author | Shtamburg, V. G. | en |
dc.contributor.author | Kostyanovsky, R. G. | en |
dc.contributor.author | Tsygankov, A. V. | en |
dc.contributor.author | Shtamburg, V. V. | en |
dc.contributor.author | Shishkin, O. V. | en |
dc.contributor.author | Zubatyuk, R. I. | en |
dc.contributor.author | Mazepa, A. V. | en |
dc.contributor.author | Kravchenko, S. V. | en |
dc.date.accessioned | 2018-06-26T09:49:02Z | |
dc.date.available | 2018-06-26T09:49:02Z | |
dc.date.issued | 2015 | |
dc.description.abstract | Molecular 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.citation | Geminal 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.uri | https://repository.kpi.kharkov.ua/handle/KhPI-Press/36916 | |
dc.language.iso | en | |
dc.publisher | Springer and Business Media, Inc. | en |
dc.subject | N-alkoxy-N-chloroureas | en |
dc.subject | anomeric effect | en |
dc.subject | N-acyloxy-N-alkoxyureas | en |
dc.subject | N-alkoxy-N-chlorocarbamates | en |
dc.subject | alcoholysis | en |
dc.subject | ureas | en |
dc.subject | carbamates | en |
dc.title | Geminal systems 64.*N-Alkoxy-N-chloroureas and N,N-dialkoxyureas | en |
dc.type | Article | en |
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