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Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines

Galina Pavlovna Sagitullina 1
Galina Pavlovna Sagitullina
Ludmila A Lisitskaya 1
Ludmila A Lisitskaya
Marina Arturovna Vorontsova 1
Marina Arturovna Vorontsova
Reva Safarovich Sagitullin 1
Reva Safarovich Sagitullin
Published 2007-05-03
CommunicationVolume 17, Issue 3, 192-193
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Sagitullina G. P. et al. Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines // Mendeleev Communications. 2007. Vol. 17. No. 3. pp. 192-193.
GOST all authors (up to 50) Copy
Sagitullina G. P., Lisitskaya L. A., Vorontsova M. A., Sagitullin R. S. Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines // Mendeleev Communications. 2007. Vol. 17. No. 3. pp. 192-193.
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TY - JOUR
DO - 10.1016/j.mencom.2007.05.022
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.05.022
TI - Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines
T2 - Mendeleev Communications
AU - Sagitullina, Galina Pavlovna
AU - Lisitskaya, Ludmila A
AU - Vorontsova, Marina Arturovna
AU - Sagitullin, Reva Safarovich
PY - 2007
DA - 2007/05/03
PB - Mendeleev Communications
SP - 192-193
IS - 3
VL - 17
ER -
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@article{2007_Sagitullina,
author = {Galina Pavlovna Sagitullina and Ludmila A Lisitskaya and Marina Arturovna Vorontsova and Reva Safarovich Sagitullin},
title = {Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines},
journal = {Mendeleev Communications},
year = {2007},
volume = {17},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.05.022},
number = {3},
pages = {192--193},
doi = {10.1016/j.mencom.2007.05.022}
}
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Sagitullina, Galina Pavlovna, et al. “Facile synthesis of substituted 1H-pyrazolo[3,4-b]pyridines.” Mendeleev Communications, vol. 17, no. 3, May. 2007, pp. 192-193. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2007.05.022.

Abstract

Substituted 1H-pyrazolo[3,4-b]pyridines were synthesised by construction of pyrazole ring from 4-substituted 5-acetyl-2-methyl-6-(methylamino)nicotinonitriles readily available via rearrangement of 3,5-dicyanopyridinium salts.

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