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Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids

Ekaterina Vladimirovna Matveeva 1
Ekaterina Vladimirovna Matveeva
, 
Vladimir Andreevich Kozlov 1
Vladimir Andreevich Kozlov
, 
Irina Leonovna Odinets 1
Irina Leonovna Odinets
10.1016/j.mencom.2010.05.007
Published 2010-05-06
Communication , Volume 20, Issue 3, 145-147
2
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Matveeva E. V., Kozlov V. A., Odinets I. L. Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids // Mendeleev Communications. 2010. Vol. 20. No. 3. pp. 145-147.
GOST all authors (up to 50) Copy
Matveeva E. V., Kozlov V. A., Odinets I. L. Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids // Mendeleev Communications. 2010. Vol. 20. No. 3. pp. 145-147.
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TY - JOUR
DO - 10.1016/j.mencom.2010.05.007
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.05.007
TI - Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids
T2 - Mendeleev Communications
AU - Matveeva, Ekaterina Vladimirovna
AU - Kozlov, Vladimir Andreevich
AU - Odinets, Irina Leonovna
PY - 2010
DA - 2010/05/06
PB - Mendeleev Communications
SP - 145-147
IS - 3
VL - 20
ER -
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@article{2010_Matveeva,
author = {Ekaterina Vladimirovna Matveeva and Vladimir Andreevich Kozlov and Irina Leonovna Odinets},
title = {Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids},
journal = {Mendeleev Communications},
year = {2010},
volume = {20},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.05.007},
number = {3},
pages = {145--147},
doi = {10.1016/j.mencom.2010.05.007}
}
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Matveeva, Ekaterina Vladimirovna, et al. “Alteration of the course of the Michaelis–Arbuzov reaction in imidazolium ionic liquids.” Mendeleev Communications, vol. 20, no. 3, May. 2010, pp. 145-147. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2010.05.007.

Abstract

Room-temperature imidazolium ionic liquids [Rmim][X] (X=Br, BF4, NTf2) as a reaction medium change the reaction course of phosphorus(III) acid esters with primary alkyl halides, aryl bromides, and propargyl bromide to afford hydrophosphoryl compounds, products of oxidation of the starting phosphorus substrates, and 2,3-bis(phosphoryl)prop-1-enes, respectively.

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