Synthesis of benzo[c][1,7]naphthyridine derivatives Full article
| Journal | 
                                    Chemistry of Heterocyclic Compounds
                                     ISSN: 0009-3122 , E-ISSN: 1573-8353  | 
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| Output data | Year: 2019, Volume: 55, Number: 11, Pages: 1080-1086 Pages count : 7 | ||||||||
| Tags | alkylation; benzo[c][1,7]naphthyridine; electrophilic substitution; nucleophilic substitution; oxidation; reactivity | ||||||||
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                            Abstract:
                            Reactivity  of  2-methyl-6-phenylbenzo[c][1,7]naphthyridine  in  alkylation,  oxidation,  and  electrophilic  substitution  reactions  has  been studied. The reaction of 2-methyl-6-phenylbenzo[c][1,7]naphthyridines with POCl 3  yielded the previously unknown 4-chloro-2-methyl-6-phenylbenzo[c][1,7]naphthyridine. Its dehalogenation and substitution of halogen by nitrogen and sulfur nucleophiles were studied.
                        
                    
                
                        Cite:
                                Shatsauskas A.L.
    ,        Saibulina E.R.
    ,        Gatilov Y.V.
    ,        Kostyuchenko A.S.
    ,        Fisyuk A.S.
    
Synthesis of benzo[c][1,7]naphthyridine derivatives
Chemistry of Heterocyclic Compounds. 2019. V.55. N11. P.1080-1086. WOS Scopus РИНЦ
                                                                        Synthesis of benzo[c][1,7]naphthyridine derivatives
Chemistry of Heterocyclic Compounds. 2019. V.55. N11. P.1080-1086. WOS Scopus РИНЦ
                                Original:
                                        Шацаускас А.Л.
    ,        Сайбулина Э.Р.
    ,        Гатилов Ю.В.
    ,        Костюченко А.С.
    ,        Фисюк А.С.
    
Синтез производных бензо[c][1,7]нафтиридина
Химия гетероциклических соединений. 2019. Т.55. №11. С.1080-1086.
                                            
                    
                                            Синтез производных бензо[c][1,7]нафтиридина
Химия гетероциклических соединений. 2019. Т.55. №11. С.1080-1086.
                            Dates:
                            
                                                                    
                        
                    
                    | Submitted: | Sep 6, 2019 | 
| Accepted: | Oct 2, 2019 | 
                        Identifiers:
                            
                    
                    
                                            
                    
                    
                | Web of science: | WOS:000510838100007 | 
| Scopus: | 2-s2.0-85076018018 | 
| Elibrary: | 43216573 |