Halogenation of phenacylpyrimidines

Halogenation of phenacylpyrimidines Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 1987, Volume: 23, Number: 5, Pages: 550-553 Pages count : 4 DOI: 10.1007/BF00476386

Authors

Semushkina I.V. ¹ , Zagulyaeva O.A. ¹ , Mamaev V.P. ¹

Affiliations

1	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Division, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

The action of bromine and chlorine of phenacylpyrimidines yields a series of α-mono- and α,α′-dihalophenacylpyrimidines. IR, UV and PMR spectroscopy showed that, in contrast to the starting compounds, the monohalo derivatives exist in the keto form. © 1987 Plenum Publishing Corporation.

Semushkina I.V. , Zagulyaeva O.A. , Mamaev V.P.
Halogenation of phenacylpyrimidines
Chemistry of Heterocyclic Compounds. 1987. V.23. N5. P.550-553. DOI: 10.1007/BF00476386 Scopus РИНЦ

Published print:

May 1, 1987

Scopus	2-s2.0-34250101856
Elibrary	30919300
OpenAlex	W1985648679