On the Two-Route Mechanism of the Reaction of 1-Alkenes with EtMgX Catalyzed by TaCl5


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Abstract

The reaction of 1-alkenes with C2D5MgBr in the presence of TaCl5 has been studied. Basing on the distribution of the deuterium label in the alkyl chain of the regioisomeric organomagnesium compounds, a tentative mechanism of their formation as key intermediates of 3-substituted tantalocyclopentanes has been proposed. The energy profiles of the reactions of carbomagnesation and β-reductive magnesaethylation of 1-alkenes have been obtained using the DFT method.

About the authors

R. M. Sultanov

Ufa State Petroleum Technical University

Author for correspondence.
Email: sultanov55@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062

F. Sh. Khafizov

Ufa State Petroleum Technical University

Email: sultanov55@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062

I. V. Ozden

Ufa State Petroleum Technical University

Email: sultanov55@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062

N. V. Shutov

Ufa State Petroleum Technical University

Email: sultanov55@mail.ru
Russian Federation, ul. Kosmonavtov 1, Ufa, 450062

D. Sh. Sabirov

Institute of Petrochemistry and Catalysis

Email: sultanov55@mail.ru
Russian Federation, pr. Oktyabrya 141, Ufa, 450075

U. M. Dzhemilev

Institute of Petrochemistry and Catalysis

Email: sultanov55@mail.ru
Russian Federation, pr. Oktyabrya 141, Ufa, 450075

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