Abe Noritaka
            
                Affiliate Master
            
                    Yamaguchi University
        
Synthesis and cycloaddition reaction of 2a, 4, 5-triazabenz[cd]azulene derivatives
        Heterocycles Volume 26 Issue 3
        Page 767-772
        
    published_at 1987
            Title
        
        Synthesis and cycloaddition reaction of 2a, 4, 5-triazabenz[cd]azulene derivatives
        
        
    
                
                    Creators
                
                    Gomi Atsuko
                
                
            
    2a, 4, 5-triazabenz[cd]azulene derivatives (2) were synthesized by the reaction of 8-hydrazino-3-phenyl-1-azaazulenes (1) with triethyl orthoformate. 2-chloro substituted compound (2b) was easily hydrolized on silica gel and gave (2-chloro-8-imino-3-phenyl-1-aza-1, 8-dihydroazulen-1-yl)formaldehyde oxime. Reaction of 2a with dimethyl acetylenedicarboxylate gave dimethyl 1-phenyl-2a, 5-diazabenz[cd]azulene-3, 4-dicarboxylate and dimethyl (1-cyano-3-phenyl-1, 8-dihydro-1-azaazulen-8-ylideneamino)maleate.
        
        
            Languages
        
            eng
    
    
        
            Resource Type
        
        journal article
    
    
        
            Publishers
        
            日本複素環化学研究所
    
    
        
            Date Issued
        
        1987
    
    
        
            File Version
        
        Version of Record
    
    
        
            Access Rights
        
        open access
    
    
            Relations
        
            
                
                
                [ISSN]0385-5414
            
            
                
                
                [NCID]AA00663739
            
    
        
            Schools
        
            大学院医学系研究科(理学)
    
                
