Abstract
<p>The catalytic oxidative methoxycarbonylation reaction of N,N-dipropargylarylamines has been investigated. PdCl<sub>2</sub>-CuCl<sub>2</sub> 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 PdCl<sub>2</sub>-CuCl<sub>2</sub>. The structures of synthesized cyclic amino triesters are established by analysis of experimental spectra NMR <sup>1</sup>H and <sup>13</sup>C, comparison with calculated spectra of possible hypothetic structures and estimation of thermodynamics properties by Joback fragmentation and MOPAC Semi-empirical PM3 methods.</p>
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