Reaction of the dimethoxyaminyl radical with tertiary nitrosoalkanes as a method for the preparation of N-alkyl-N?-methoxydiazene N-oxides
摘要:
The reaction of the dimethoxyaminyl radical with functionally substituted nitrosoalkanes (2) in a 2:1 ratio at 20-degrees-C gives the corresponding N-alkyl-N'-methoxydiazene N-oxides (3) as a single isomer in preparative yields.
Reactions of N-chloro-N-alkoxy-tert-alkylamines with isobutylene and methanol
作者:V. G. Shtamburg、V. F. Rudchenko、V. M. Grinev、A. A. Dmitrenko、A. P. Pleshkova、R. G. Kostyanovskii
DOI:10.1007/bf00961356
日期:1991.5
The addition of N-chloro-N-methoxy-tert-alkylamines to an olefin, which is assumed to proceed with the participation of alkoxynitrenium ions, was carried out for the first time. The methanolysis of N-chloro-N-alkoxy-tert-alkylamines in the presence of Et3N gives dialkoxyamines, and depending on the type of the N-alkyl substituent is accompanied by side reactions.
SHTAMBURG, V. G.;RUDCHENKO, V. F.;GRINEV, V. M.;DMITRENKO, A. A.;PLESHKOV+, IZV. AN CCCP. CEP. XIM.,(1991) N, S. 1069-1072
作者:SHTAMBURG, V. G.、RUDCHENKO, V. F.、GRINEV, V. M.、DMITRENKO, A. A.、PLESHKOV+
DOI:——
日期:——
Peracid oxidation of imino ethers
作者:Donald H. Aue、Darryl Thomas
DOI:10.1021/jo00940a012
日期:1974.12
Reaction of the dimethoxyaminyl radical with tertiary nitrosoalkanes as a method for the preparation of N-alkyl-N?-methoxydiazene N-oxides
作者:V. F. Rudchenko、S. M. Ignatov、R. G. Kostyanovskii
DOI:10.1007/bf00863834
日期:1992.10
The reaction of the dimethoxyaminyl radical with functionally substituted nitrosoalkanes (2) in a 2:1 ratio at 20-degrees-C gives the corresponding N-alkyl-N'-methoxydiazene N-oxides (3) as a single isomer in preparative yields.