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Chemical properties of ylidene derivatives of azines. 1. Structure of the products of protonation of dihydro-2-pyrimidylidene- and dihydro-4-pyrimidylidenecyanoacetic esters Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 1982, Volume: 18, Number: 3, Pages: 300-306 Pages count : DOI: 10.1007/BF00522135
Authors Zagulyaeva O. A. , Grigorkina O. A. , Mamatyuk V. I. , Mamaev V. P.
Affiliations
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

Abstract: The structure of the products of protonation of dihydro-2-pyrimidylidene- and dihydro-4-pyrimidylidenecyanoacetic esters was investigated by means of IR, UV, and 1H and 13C NMR spectroscopy. It is shown that, in contrast to the corresponding α-derivative of pyridine. the investigated compounds have an ylidene structure in solutions of strong acids and in the form of perchlorates; the protons are attached to the heterocyclic nitrogen atoms. © 1982 Plenum Publishing Corporation.
Cite: Zagulyaeva O.A. , Grigorkina O.A. , Mamatyuk V.I. , Mamaev V.P.
Chemical properties of ylidene derivatives of azines. 1. Structure of the products of protonation of dihydro-2-pyrimidylidene- and dihydro-4-pyrimidylidenecyanoacetic esters
Chemistry of Heterocyclic Compounds. 1982. V.18. N3. P.300-306. DOI: 10.1007/BF00522135 Scopus РИНЦ OpenAlex
Dates:
Published print: Mar 1, 1982
Identifiers:
Scopus: 2-s2.0-34250233240
Elibrary: 30832717
OpenAlex: W2063149884
Citing: Пока нет цитирований
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