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 | ||
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| Output data | Year: 1965, Volume: 14, Number: 11, Pages: 2043-2045 Pages count : 3 DOI: 10.1007/BF00845916 | ||
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                            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
                    
                    
                                            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 | 
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