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

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

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.

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

Published print:

Jan 1, 1994

Web of science	WOS:A1994NR82700007
Scopus	2-s2.0-84930940046
Elibrary	30970584
OpenAlex	W2950995925