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Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole

Igor L'vovich Dalinger 1
Igor L'vovich Dalinger
Irina Anatol'evna Vatsadze 1
Irina Anatol'evna Vatsadze
Tatiana Konstantinovna Shkineva 1
Tatiana Konstantinovna Shkineva
Galina Pavlovna Popova 1
Galina Pavlovna Popova
Svyatoslav Arkad'evich Shevelev 1
Svyatoslav Arkad'evich Shevelev
Published 2011-04-28
CommunicationVolume 21, Issue 3, 149-150
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Dalinger I. L. et al. Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole // Mendeleev Communications. 2011. Vol. 21. No. 3. pp. 149-150.
GOST all authors (up to 50) Copy
Dalinger I. L., Vatsadze I. A., Shkineva T. K., Popova G. P., Shevelev S. A. Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole // Mendeleev Communications. 2011. Vol. 21. No. 3. pp. 149-150.
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TY - JOUR
DO - 10.1016/j.mencom.2011.04.012
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.04.012
TI - Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole
T2 - Mendeleev Communications
AU - Dalinger, Igor L'vovich
AU - Vatsadze, Irina Anatol'evna
AU - Shkineva, Tatiana Konstantinovna
AU - Popova, Galina Pavlovna
AU - Shevelev, Svyatoslav Arkad'evich
PY - 2011
DA - 2011/04/28
PB - Mendeleev Communications
SP - 149-150
IS - 3
VL - 21
ER -
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@article{2011_Dalinger,
author = {Igor L'vovich Dalinger and Irina Anatol'evna Vatsadze and Tatiana Konstantinovna Shkineva and Galina Pavlovna Popova and Svyatoslav Arkad'evich Shevelev},
title = {Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole},
journal = {Mendeleev Communications},
year = {2011},
volume = {21},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.04.012},
number = {3},
pages = {149--150},
doi = {10.1016/j.mencom.2011.04.012}
}
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Dalinger, Igor L'vovich, et al. “Nucleophilic substitution in 1-methyl-3,4,5-trinitro-1H-pyrazole.” Mendeleev Communications, vol. 21, no. 3, Apr. 2011, pp. 149-150. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2011.04.012.

Abstract

1-Methyl-3,4,5-trinitropyrazole in reaction with thiols, phenols, oximes, ammonia, amines and NH-azoles gives substitution products of the 5-positioned nitro group.

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