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Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide

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Kornev M. Y. et al. Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 72-74.
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Kornev M. Y., Moshkin V. S., Eltsov O. S., Sosnovskikh V. Y. Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide // Mendeleev Communications. 2015. Vol. 26. No. 1. pp. 72-74.
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TY - JOUR
DO - 10.1016/j.mencom.2016.01.028
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.028
TI - Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide
T2 - Mendeleev Communications
AU - Kornev, Mikhail Yur'evich
AU - Moshkin, Vladimir Sergeevich
AU - Eltsov, Oleg Stanislavovich
AU - Sosnovskikh, Vyacheslav Yakovlevich
PY - 2015
DA - 2015/12/30
PB - Mendeleev Communications
SP - 72-74
IS - 1
VL - 26
ER -
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@article{2015_Kornev,
author = {Mikhail Yur'evich Kornev and Vladimir Sergeevich Moshkin and Oleg Stanislavovich Eltsov and Vyacheslav Yakovlevich Sosnovskikh},
title = {Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide},
journal = {Mendeleev Communications},
year = {2015},
volume = {26},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.028},
number = {1},
pages = {72--74},
doi = {10.1016/j.mencom.2016.01.028}
}
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Kornev, Mikhail Yur'evich, et al. “Reactions of chromone-3-carboxylic acid and chromone-3-carboxamides with cyanoacetic acid hydrazide.” Mendeleev Communications, vol. 26, no. 1, Dec. 2015, pp. 72-74. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.01.028.

Abstract

Chromone and chromone-3-carboxylic acid react with cyanoacetic acid hydrazide in the presence of NaOEt in boiling ethanol to form 6-(2-hydroxyphenyl)-1H-pyrazolo[3,4-b]pyridin-3(2H)-one (58–62% yields), whereas reaction between chromone-3-carboxamides and cyanoacetic acid hydrazide under the same conditions affords 1-amino-2,5-dioxo-2,5-dihydro-1H-chromeno[4,3-b]pyridine-3-carbonitriles (50–67% yields).

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