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4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions

Alexey Vladimirovich Smirnov 1
Alexey Vladimirovich Smirnov
,  , 
Vladimir Vladimirovich Plakhtinskii 1
Vladimir Vladimirovich Plakhtinskii
, 
Galina Grigor'evna Krasovskaya 1
Galina Grigor'evna Krasovskaya
10.1070/MC2002v012n02ABEH001538
Published 2002-04-30
Communication , Volume 12, Issue 2, 72-74
13
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Smirnov A. V. et al. 4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions // Mendeleev Communications. 2002. Vol. 12. No. 2. pp. 72-74.
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Smirnov A. V., Abramov I. G., Plakhtinskii V. V., Krasovskaya G. G. 4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions // Mendeleev Communications. 2002. Vol. 12. No. 2. pp. 72-74.
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TY - JOUR
DO - 10.1070/MC2002v012n02ABEH001538
UR - https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001538
TI - 4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions
T2 - Mendeleev Communications
AU - Smirnov, Alexey Vladimirovich
AU - Abramov, Igor Gennad'evich
AU - Plakhtinskii, Vladimir Vladimirovich
AU - Krasovskaya, Galina Grigor'evna
PY - 2002
DA - 2002/04/30
PB - Mendeleev Communications
SP - 72-74
IS - 2
VL - 12
ER -
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@article{2002_Smirnov,
author = {Alexey Vladimirovich Smirnov and Igor Gennad'evich Abramov and Vladimir Vladimirovich Plakhtinskii and Galina Grigor'evna Krasovskaya},
title = {4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions},
journal = {Mendeleev Communications},
year = {2002},
volume = {12},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001538},
number = {2},
pages = {72--74},
doi = {10.1070/MC2002v012n02ABEH001538}
}
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Smirnov, Alexey Vladimirovich, et al. “4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions.” Mendeleev Communications, vol. 12, no. 2, Apr. 2002, pp. 72-74. https://mendcomm.colab.ws/publications/10.1070/MC2002v012n02ABEH001538.

Abstract

The title compound was synthesised, and its derivatives were prepared in high yields using the selective substitution of O-, S- and N-nucleophiles for the nitro group; an activating effect of the benzotriazolyl moiety on the above reactions was found.

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