Alcoholysis of N-acetoxy-N-alkoxycarbamates. Synthesis of NH-N,N-dialkoxyamines from N,N-dialkoxycarbamates
dc.contributor.author | Shtamburg, V. G. | en |
dc.contributor.author | Anishchenko, A. A. | en |
dc.contributor.author | Shtamburg, V. V. | en |
dc.contributor.author | Tsygankov, A. V. | en |
dc.contributor.author | Kostyanovsky, R. G. | en |
dc.date.accessioned | 2018-06-25T12:34:58Z | |
dc.date.available | 2018-06-25T12:34:58Z | |
dc.date.issued | 2014 | |
dc.description.abstract | The alcoholysis of N-acetoxy-N-alkoxycarbamates by methanol or ethanol at 20 – 40 °C yields N,N-dialkoxycarbamates and acetic acid. At the lower temperature the competitive formation of N,N’-bis(alkoxycarbonyl)-N,N’-bis(alkoxy)hydrazines can occur. The alkaline hydrolysis of N,N-dialkoxycarbamates yields NH-N,N-dialkoxyamines. | en |
dc.identifier.citation | Alcoholysis of N-acetoxy-N-alkoxycarbamates. Synthesis of NH-N,N-dialkoxyamines from N,N-dialkoxycarbamates / V. G. Shtamburg [et al.] // European Chemical Bulletin. – 2014. – Vol. 3, № 12. – P. 1119-1125. | en |
dc.identifier.uri | https://repository.kpi.kharkov.ua/handle/KhPI-Press/36903 | |
dc.language.iso | en | |
dc.publisher | Deuton-X Ltd. | en |
dc.subject | nucleophilic substitution | en |
dc.subject | nitrogen | en |
dc.subject | N-acyloxy-N-alkoxycarbamates | en |
dc.subject | alcoholysis | en |
dc.subject | N,N-dialkoxycarbamates | en |
dc.subject | hydrolysis | en |
dc.title | Alcoholysis of N-acetoxy-N-alkoxycarbamates. Synthesis of NH-N,N-dialkoxyamines from N,N-dialkoxycarbamates | en |
dc.type | Article | en |
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