Oxidative Carbonylation of Dipropargylarylamines

The catalytic oxidative methoxycarbonylation reaction of N,N-dipropargylarylamines has been investigated. PdCl2-CuCl2 has been studied as a catalytic system. Consecutive reactions of substitutive and additive methoxycarbonylation have been going in this process, which has been complicated by dimeris...

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Main Authors: S. A. Vizer, K. B. Yerzhanov, Z. N. Manchuk, A. G. Wieser
Format: Article
Language:English
Published: al-Farabi Kazakh National University 1999-11-01
Series:Eurasian Chemico-Technological Journal 
Online Access:http://ect-journal.kz/index.php/ectj/article/view/1
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spelling doaj-532798a56eea4706b8314bf15800bd482020-11-24T22:00:32Zengal-Farabi Kazakh National UniversityEurasian Chemico-Technological Journal 1562-39202522-48671999-11-01111810.18321/ectj3411Oxidative Carbonylation of DipropargylarylaminesS. A. Vizer0K. B. Yerzhanov1Z. N. Manchuk2A. G. Wieser3Institute of Chemical Sciences ME&S RK 106, Sh. Walikhanov st., Almaty, 480100, KazakhstanInstitute of Chemical Sciences ME&S RK 106, Sh. Walikhanov st., Almaty, 480100, KazakhstanInstitute of Chemical Sciences ME&S RK 106, Sh. Walikhanov st., Almaty, 480100, KazakhstanInstitute of Chemical Sciences ME&S RK 106, Sh. Walikhanov st., Almaty, 480100, KazakhstanThe catalytic oxidative methoxycarbonylation reaction of N,N-dipropargylarylamines has been investigated. PdCl2-CuCl2 has been studied as a catalytic system. Consecutive reactions of substitutive and additive methoxycarbonylation have been going in this process, which has been complicated by dimerisation, polymerization and cyclization processes. Apparently the results of process are determined by stability of intermediate reactionary complexes with participation of catalytic system PdCl2-CuCl2. The structures of synthesized cyclic amino triesters are established by analysis of experimental spectra NMR 1H and 13C, comparison with calculated spectra of possible hypothetic structures and estimation of thermodynamics properties by Joback fragmentation and MOPAC Semi-empirical PM3 methods.http://ect-journal.kz/index.php/ectj/article/view/1
collection DOAJ
language English
format Article
sources DOAJ
author S. A. Vizer
K. B. Yerzhanov
Z. N. Manchuk
A. G. Wieser
spellingShingle S. A. Vizer
K. B. Yerzhanov
Z. N. Manchuk
A. G. Wieser
Oxidative Carbonylation of Dipropargylarylamines
Eurasian Chemico-Technological Journal 
author_facet S. A. Vizer
K. B. Yerzhanov
Z. N. Manchuk
A. G. Wieser
author_sort S. A. Vizer
title Oxidative Carbonylation of Dipropargylarylamines
title_short Oxidative Carbonylation of Dipropargylarylamines
title_full Oxidative Carbonylation of Dipropargylarylamines
title_fullStr Oxidative Carbonylation of Dipropargylarylamines
title_full_unstemmed Oxidative Carbonylation of Dipropargylarylamines
title_sort oxidative carbonylation of dipropargylarylamines
publisher al-Farabi Kazakh National University
series Eurasian Chemico-Technological Journal 
issn 1562-3920
2522-4867
publishDate 1999-11-01
description The catalytic oxidative methoxycarbonylation reaction of N,N-dipropargylarylamines has been investigated. PdCl2-CuCl2 has been studied as a catalytic system. Consecutive reactions of substitutive and additive methoxycarbonylation have been going in this process, which has been complicated by dimerisation, polymerization and cyclization processes. Apparently the results of process are determined by stability of intermediate reactionary complexes with participation of catalytic system PdCl2-CuCl2. The structures of synthesized cyclic amino triesters are established by analysis of experimental spectra NMR 1H and 13C, comparison with calculated spectra of possible hypothetic structures and estimation of thermodynamics properties by Joback fragmentation and MOPAC Semi-empirical PM3 methods.
url http://ect-journal.kz/index.php/ectj/article/view/1
work_keys_str_mv AT savizer oxidativecarbonylationofdipropargylarylamines
AT kbyerzhanov oxidativecarbonylationofdipropargylarylamines
AT znmanchuk oxidativecarbonylationofdipropargylarylamines
AT agwieser oxidativecarbonylationofdipropargylarylamines
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