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Reaction between phthalonitrile and phenylacetonitrile

Vladimir Yur'evich Orlov 1
Vladimir Yur'evich Orlov
, 
Aleksandr Dmitrievich Kotov 1
Aleksandr Dmitrievich Kotov
, 
Nikolay Aleksandrovich Budanov 1
Nikolay Aleksandrovich Budanov
10.1070/MC2000v010n02ABEH001213
Published 2000-03-30
Communication , Volume 10, Issue 2, 76-77
2
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Orlov V. Y., Kotov A. D., Budanov N. A. Reaction between phthalonitrile and phenylacetonitrile // Mendeleev Communications. 2000. Vol. 10. No. 2. pp. 76-77.
GOST all authors (up to 50) Copy
Orlov V. Y., Kotov A. D., Budanov N. A. Reaction between phthalonitrile and phenylacetonitrile // Mendeleev Communications. 2000. Vol. 10. No. 2. pp. 76-77.
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TY - JOUR
DO - 10.1070/MC2000v010n02ABEH001213
UR - https://mendcomm.colab.ws/publications/10.1070/MC2000v010n02ABEH001213
TI - Reaction between phthalonitrile and phenylacetonitrile
T2 - Mendeleev Communications
AU - Orlov, Vladimir Yur'evich
AU - Kotov, Aleksandr Dmitrievich
AU - Budanov, Nikolay Aleksandrovich
PY - 2000
DA - 2000/03/30
PB - Mendeleev Communications
SP - 76-77
IS - 2
VL - 10
ER -
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@article{2000_Orlov,
author = {Vladimir Yur'evich Orlov and Aleksandr Dmitrievich Kotov and Nikolay Aleksandrovich Budanov},
title = {Reaction between phthalonitrile and phenylacetonitrile},
journal = {Mendeleev Communications},
year = {2000},
volume = {10},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2000v010n02ABEH001213},
number = {2},
pages = {76--77},
doi = {10.1070/MC2000v010n02ABEH001213}
}
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Orlov, Vladimir Yur'evich, et al. “Reaction between phthalonitrile and phenylacetonitrile.” Mendeleev Communications, vol. 10, no. 2, Mar. 2000, pp. 76-77. https://mendcomm.colab.ws/publications/10.1070/MC2000v010n02ABEH001213.

Abstract

The title reaction performed in the DMSO–NaOH system resulted in the formation of 2,3-diphenyl-2,3-(2′-cyanophenyl)butanedioic acid diamide, which was selectively hydrolysed to 2,3-diphenyl-2,3-(2′-cyanophenyl)butanedioic acid.

References

1.
10.1070/MC2000v010n02ABEH001213_bib1
Terrier
Nucleophilic Aromatic Displacement: The Influence of the Nitro Group, 1991
2.
10.1070/MC2000v010n02ABEH001213_bib2
Kaninskii
Zh. Org. Khim., 1992
3.
10.1070/MC2000v010n02ABEH001213_bib3
Plahtinskii
Kinet. Katal., 1993
4.
10.1070/MC2000v010n02ABEH001213_bib4
Bardin
Izv. Sib. Otd. Akad. Nauk SSSR, Ser. Khim. Nauk, 1988
5.
Vicarious nucleophilic substitution of hydrogen
Makosza M., Winiarski J.
Accounts of Chemical Research, 1987
6.
10.1070/MC2000v010n02ABEH001213_bib6
Chupakhin
Nucleophilic Aromatic Substitution of Hydrogen, 1994
8.
10.1070/MC2000v010n02ABEH001213_bib8
Kopeykin
Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol., 1992
9.
10.1070/MC2000v010n02ABEH001213_bib9
Roze
Zh. Org. Khim., 1987