Synthesis of hybrid molecules containing pyrimidine and diterpene alkaloid lappaconitine fragments Full article
| Journal | Chemistry of Heterocyclic Compounds ISSN: 0009-3122 , E-ISSN: 1573-8353 | ||||
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| Output data | Year: 2018, Volume: 54, Number: 12, Pages: 1131-1138 Pages count : 8 DOI: 10.1007/s10593-019-02404-w | ||||
| Tags | alkaloids; alkynes; amidines; pyrimidines; cross coupling; one-pot synthesis | ||||
| Authors |  | ||||
| Affiliations | 
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                            Abstract:
                            The cross coupling of 5'-ethynyllappaconitine with benzoic acid chlorides under the conditions of the Sonogashira reaction in benzene leads to the corresponding 5-alkynones. By condensation of the obtained 5'-alkynones with amidines, compounds with hybrid structure containing fragments of a diterpene alkaloid and pyrimidine were synthesized. The yields of the target compounds were 67-90%. The possibility of carrying out the cross coupling - condensation reaction as a one-pot synthesis is demonstrated.
                        
                    
                
                        Cite:
                                Cheremnykh K.P.
    ,        Savel'ev V.A.
    ,        Shkurko O.P.
    ,        Shults E.E.
    
Synthesis of hybrid molecules containing pyrimidine and diterpene alkaloid lappaconitine fragments
Chemistry of Heterocyclic Compounds. 2018. V.54. N12. P.1131-1138. DOI: 10.1007/s10593-019-02404-w WOS Scopus РИНЦ OpenAlex
                    
                    
                                            Synthesis of hybrid molecules containing pyrimidine and diterpene alkaloid lappaconitine fragments
Chemistry of Heterocyclic Compounds. 2018. V.54. N12. P.1131-1138. DOI: 10.1007/s10593-019-02404-w WOS Scopus РИНЦ OpenAlex
                            Dates:
                            
                                                                    
                        
                    
                    | Published print: | Dec 1, 2018 | 
| Published online: | Jan 18, 2019 | 
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                | Web of science: | WOS:000461553300008 | 
| Scopus: | 2-s2.0-85060186594 | 
| Elibrary: | 38667200 | 
| OpenAlex: | W2909181259 |