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

Journal Mendeleev Communications
ISSN: 0959-9436
Output data Year: 1994, Volume: 4, Number: 2, Pages: 50-51 Pages count : 2 DOI: 10.1070/MC1994v004n02ABEH000343
Authors Oleinik I.V. 1 , Zagulyaeva O.A. 1
Affiliations
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, 630090, Russian Federation

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. © 1994, jointly by The Russian Academy of Sciences and The Royal Society of Chemistry (Turpion Ltd). All rights reserved.
Cite: 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. V.4. N2. P.50-51. DOI: 10.1070/MC1994v004n02ABEH000343 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Jan 1, 1994
Identifiers:
Web of science: WOS:A1994NR82700007
Scopus: 2-s2.0-84930940046
Elibrary: 30970584
OpenAlex: W2950995925
Citing:
DB Citing
Scopus 4
Web of science 3
Elibrary 3
OpenAlex 5
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