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

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

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.

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

Published print:

Nov 1, 1965

Scopus	2-s2.0-34250604148
OpenAlex	W2069208834