A facile approach to hybrid compounds containing a tricyclic diterpenoid and fluorine-substituted heterocycles Научная публикация
| Журнал | Journal of Fluorine Chemistry ISSN: 0022-1139 | ||||
|---|---|---|---|---|---|
| Вых. Данные | Год: 2020, Том: 236, Номер статьи : 109554, Страниц : DOI: 10.1016/j.jfluchem.2020.109554 | ||||
| Ключевые слова | Fluorinated heterocycles; 2H-chromenes; Benzofurans; Isopimaric acid; Terpenoid allene; Cross-coupling-cyclization | ||||
| Авторы |  | ||||
| Организации | 
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                            Реферат:
                            2,3-Butadienes have become valuable building blocks in the synthesis of various heterocyclic compounds. The Pd-catalyzed cross-coupling and cyclization reaction of N-(2,3-butadienyl)carboxamide of isopimaric acid with fluorine-substituted 2-iodophenols proceeds with the formation of optically active fluorinated benzofuran and benzopyrane derivatives of isopimaric acid. This transformation opens a potential route to the synthesis of hybrid compounds containing a tricyclic diterpenoid moiety and several fluorinated benzoannelated heterocycles.
                        
                    
                
                        Библиографическая ссылка:
                                Gromova M.A.
    ,        Kharitonov Y.V.
    ,        Politanskaya L.,.V.
    ,        Tretyakov E.,.V.
    ,        Shults E.E.
    
A facile approach to hybrid compounds containing a tricyclic diterpenoid and fluorine-substituted heterocycles
Journal of Fluorine Chemistry. 2020. V.236. 109554 . DOI: 10.1016/j.jfluchem.2020.109554 WOS Scopus РИНЦ OpenAlex
                    
                    
                                            A facile approach to hybrid compounds containing a tricyclic diterpenoid and fluorine-substituted heterocycles
Journal of Fluorine Chemistry. 2020. V.236. 109554 . DOI: 10.1016/j.jfluchem.2020.109554 WOS Scopus РИНЦ OpenAlex
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                    | Опубликована в печати: | 1 авг. 2020 г. | 
                        Идентификаторы БД:
                            
                    
                    
                                            
                    
                                            
                    
                | Web of science: | WOS:000551145100004 | 
| Scopus: | 2-s2.0-85085295681 | 
| РИНЦ: | 43293186 | 
| OpenAlex: | W3025522951 |