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Synthesis of substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones

Valeria Anatol'evna Panova 1
Valeria Anatol'evna Panova
Mikhail Konstantinovich Korsakov 1
Mikhail Konstantinovich Korsakov
Anton Andreevich Shetnev 1
Anton Andreevich Shetnev
Sergey Ivanovich Filimonov 1
Sergey Ivanovich Filimonov
Published 2018-12-28
CommunicationVolume 29, Issue 1, 114-115
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Panova V. A. et al. Synthesis of substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones // Mendeleev Communications. 2018. Vol. 29. No. 1. pp. 114-115.
GOST all authors (up to 50) Copy
Panova V. A., Korsakov M. K., Shetnev A. A., Filimonov S. I. Synthesis of substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones // Mendeleev Communications. 2018. Vol. 29. No. 1. pp. 114-115.
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TY - JOUR
DO - 10.1016/j.mencom.2019.01.039
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.01.039
TI - Synthesis of substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones
T2 - Mendeleev Communications
AU - Panova, Valeria Anatol'evna
AU - Korsakov, Mikhail Konstantinovich
AU - Shetnev, Anton Andreevich
AU - Filimonov, Sergey Ivanovich
PY - 2018
DA - 2018/12/28
PB - Mendeleev Communications
SP - 114-115
IS - 1
VL - 29
ER -
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@article{2018_Panova,
author = {Valeria Anatol'evna Panova and Mikhail Konstantinovich Korsakov and Anton Andreevich Shetnev and Sergey Ivanovich Filimonov},
title = {Synthesis of substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones},
journal = {Mendeleev Communications},
year = {2018},
volume = {29},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.01.039},
number = {1},
pages = {114--115},
doi = {10.1016/j.mencom.2019.01.039}
}
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Panova, Valeria Anatol'evna, et al. “Synthesis of substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones.” Mendeleev Communications, vol. 29, no. 1, Dec. 2018, pp. 114-115. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.01.039.

Abstract

A two-stage selective synthesis of new substituted 5-hydroxypyrazolo[1,5-a]quinoxalin-4-ones from ethyl 3-arylpyrazole-5-carboxylates and activated o-chloronitroarenes substrates has been developed.

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