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Azo-coupling reaction of anthra-1,3-oxazines with aromatic diazo compounds Full article

Journal Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
ISSN: 0568-5230
Output data Year: 1965, Volume: 14, Number: 11, Pages: 2043-2045 Pages count : 3 DOI: 10.1007/BF00845916
Authors Fokin E.P. 1 , Denisov V.Ya. 1
Affiliations
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Section of the Academy of Sciences of the USSR

Abstract: 1. The acyl derivatives of anthra-1,3-oxazine (I) enter into the azo-coupling reaction with aromatic diazo compounds; here the diazo group enters in the p-position to the tertiary nitrogen atom of the anthra-1,3-oxazine. 2. The arylazoanthra-1,3-oxazines (II) by hydrolytic cleavage of the 1,3-oxazine ring and the action of air are converted to the arylazo derivatives of N-1-anthraquinonyl-δ-aminovaleraldehyde. © 1966 Consultants Bureau.
Cite: Fokin E.P. , Denisov V.Y.
Azo-coupling reaction of anthra-1,3-oxazines with aromatic diazo compounds
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 1965. V.14. N11. P.2043-2045. DOI: 10.1007/BF00845916 Scopus OpenAlex
Dates:
Published print: Nov 1, 1965
Identifiers:
Scopus: 2-s2.0-34250604148
OpenAlex: W2069208834
Citing: Пока нет цитирований
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