Home / Publications / Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans

Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans

, 
Margarita Alekseevna Epishina 1
Margarita Alekseevna Epishina
, 
Alexander Sergeyevich Kulikov 1
Alexander Sergeyevich Kulikov
, 
Nina Nikolaevna Makhova 1
Nina Nikolaevna Makhova
10.1016/j.mencom.2015.01.013
Published 2014-12-26
Communication , Volume 25, Issue 1, 36-38
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Fershtat L. L. et al. Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans // Mendeleev Communications. 2014. Vol. 25. No. 1. pp. 36-38.
GOST all authors (up to 50) Copy
Fershtat L. L., Epishina M. A., Kulikov A. S., Makhova N. N. Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans // Mendeleev Communications. 2014. Vol. 25. No. 1. pp. 36-38.
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TY - JOUR
DO - 10.1016/j.mencom.2015.01.013
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.01.013
TI - Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans
T2 - Mendeleev Communications
AU - Fershtat, Leonid Leonidovich
AU - Epishina, Margarita Alekseevna
AU - Kulikov, Alexander Sergeyevich
AU - Makhova, Nina Nikolaevna
PY - 2014
DA - 2014/12/26
PB - Mendeleev Communications
SP - 36-38
IS - 1
VL - 25
ER -
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@article{2014_Fershtat,
author = {Leonid Leonidovich Fershtat and Margarita Alekseevna Epishina and Alexander Sergeyevich Kulikov and Nina Nikolaevna Makhova},
title = {Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans},
journal = {Mendeleev Communications},
year = {2014},
volume = {25},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.01.013},
number = {1},
pages = {36--38},
doi = {10.1016/j.mencom.2015.01.013}
}
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Fershtat, Leonid Leonidovich, et al. “Design of hetarylthiofuroxans by nucleophilic substitution of NO2 group in nitrofuroxans.” Mendeleev Communications, vol. 25, no. 1, Dec. 2014, pp. 36-38. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.01.013.

Abstract

Hetarylthiofuroxans were synthesized by nucleophilic substitution of the nitro group in 4-nitrofuroxans under the action of hetarylthiols in the DBU–MeCN system at room temperature, reactivity of 4-nitrofuroxans being dependent on the C(3)-substituent.

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