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Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles

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Oleinik I. V., Zagulyaeva O. A. Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles // Mendeleev Communications. 1994. Vol. 4. No. 2. pp. 50-51.
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Oleinik I. V., Zagulyaeva O. A. Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles // Mendeleev Communications. 1994. Vol. 4. No. 2. pp. 50-51.
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TY - JOUR
DO - 10.1070/MC1994v004n02ABEH000343
UR - https://mendcomm.colab.ws/publications/10.1070/MC1994v004n02ABEH000343
TI - Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles
T2 - Mendeleev Communications
AU - Oleinik, Irina V
AU - Zagulyaeva, Olga Alekseevna
PY - 1994
DA - 1994/04/30
PB - Mendeleev Communications
SP - 50-51
IS - 2
VL - 4
ER -
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@article{1994_Oleinik,
author = {Irina V Oleinik and Olga Alekseevna Zagulyaeva},
title = {Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles},
journal = {Mendeleev Communications},
year = {1994},
volume = {4},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1994v004n02ABEH000343},
number = {2},
pages = {50--51},
doi = {10.1070/MC1994v004n02ABEH000343}
}
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Oleinik, Irina V., and Olga Alekseevna Zagulyaeva. “Reaction of Dihydroazinylidene Cyanoacetic Esters with Nitric Acid: A New Method for the Synthesis of Dihydroazinylidene Nitroacetonitriles.” Mendeleev Communications, vol. 4, no. 2, Apr. 1994, pp. 50-51. https://mendcomm.colab.ws/publications/10.1070/MC1994v004n02ABEH000343.

Abstract

An approach to the synthesis of previously unknown dihydroazinylidene nitroacetonitriles (derivatives of pyridine, pyrimidine, pyrazine and pyridazine) has been developed involving nitration of the corresponding dihydroazinylidene cyanoacetic esters at the side chain α-C-atom and dealkoxycarbonylation of the resulting products.

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