Palladium-Catalyzed Regioselective Alkenylation of Flavone Derivatives

References

1. Pieroni A. Pachaly P. Huang Y. Van Poel B. Vlietinck A.J. J. Ethnopharmacol. 2000 70 3 213 217 10.1016/S0378‑8741(99)00169‑5 10837985
   [Google Scholar]
2. Frum Y. Viljoen A.M. Van Heerden F.R. S. Afr. J. Bot. 2007 73 4 583 587 10.1016/j.sajb.2007.05.006
   [Google Scholar]
3. Sharma A. Gupta S. Chauhan S. Nair A. Sharma P. Pharmacol. Res. 2020 158 104894 10.1016/j.phrs.2020.104894 32407960
   [Google Scholar]
4. Cao J. Xia X. Chen X. Xiao J. Wang Q. Food Chem. Toxicol. 2013 51 242 250 10.1016/j.fct.2012.09.039 23063594
   [Google Scholar]
5. Yu W. Sun H. Zha W. Cui W. Xu L. Min Q. Wu J. Evid. Based Complement. Alternat. Med. 2017 2017 1 2590676 10.1155/2017/2590676 28684964
   [Google Scholar]
6. Yang Y.Z. Tang Y.Z. Liu Y.H. J. Ethnopharmacol. 2013 148 1 271 276 10.1016/j.jep.2013.04.025 23612420
   [Google Scholar]
7. He J. Hu Z. Dong Z. Li B. Chen K. Shang Z. Zhang M. Qiao X. Ye M. Adv. Synth. Catal. 2020 362 3 528 532 10.1002/adsc.201901396
   [Google Scholar]
8. Bao S. Luo L. Wan Y. Xu K. Tan G. Fan J. Li S.M. Yu X. Bioorg. Chem. 2021 110 104787 10.1016/j.bioorg.2021.104787 33711657
   [Google Scholar]
9. Chen R. Liu X. Zou J. Yin Y. Ou B. Li J. Wang R. Xie D. Zhang P. Dai. J. Adv. Synth. Catal. 2013 355 9 1817 1828 10.1002/adsc.201300196
   [Google Scholar]
10. Tischer S. Metz P. Adv. Synth. Catal. 2007 349 1-2 147 151 10.1002/adsc.200600454
    [Google Scholar]
11. Khodzhaieva R.S. Gladkov E.S. Kyrychenko A. Roshal A.D. Front Chem. 2021 9 637994 10.3389/fchem.2021.637994 33869141
    [Google Scholar]
12. Hofer B. Appl. Microbiol. Biotechnol. 2016 100 10 4269 4281 10.1007/s00253‑016‑7465‑0 27029191
    [Google Scholar]
13. Xiao J. Muzashvili T.S. Georgiev M.I. Biotechnol. Adv. 2014 32 6 1145 1156 10.1016/j.biotechadv.2014.04.006 24780153
    [Google Scholar]
14. Hui-Yao G. Yan L. Fei-Fan T. Li-Wen Z. Kai-Zhi J. Ya-Jie T. Curr. Pharm. Des. 2022 28 1466 1479 10.2174/1381612828666220422085128 35466866
    [Google Scholar]
15. Lin C.F. Lin M.H. Hung C.F. Alshetaili A. Tsai Y.F. Jhong C.L. Fang J.Y. Phytother. Res. 2024 38 4 1951 1970 10.1002/ptr.8140 38358770
    [Google Scholar]
16. de Araújo M. Franco Y. Messias M. Longato G. Pamphile J. Carvalho P. Planta Med. 2016 83 01/02 7 22 10.1055/s‑0042‑118883 27919108
    [Google Scholar]
17. Islam A. Islam M.S. Rahman M.K. Uddin M.N. Akanda M.R. Arch. Pharm. Res. 2020 43 6 582 592 10.1007/s12272‑020‑01243‑0 32594426
    [Google Scholar]
18. Fesen M.R. Pommier Y. Leteurtre F. Hiroguchi S. Yung J. Kohn K.W. Biochem. Pharmacol. 1994 48 3 595 608 10.1016/0006‑2952(94)90291‑7 7520698
    [Google Scholar]
19. Shi Y.J. Gao J.W. Liu C.F. J. Mol. Struct. 2022 1268 133674 10.1016/j.molstruc.2022.133674
    [Google Scholar]
20. Gao J.W. Zhao Y.P. Shi Y.J. Liu C.F. J. Mol. Struct. 2025 1320 139736 10.1016/j.molstruc.2024.139736
    [Google Scholar]
21. Zhao Y.P. Liao J.L. Liu C.F. Tetrahedron Lett. 2023 123 154573 10.1016/j.tetlet.2023.154573
    [Google Scholar]
22. Fekete S. Patonay T. Silva A.M.S. Cavaleiro J.A.S. ARKIVOC 2012 2012 5 210 225 10.3998/ark.5550190.0013.519
    [Google Scholar]
23. Ma Y. Yin D. Ye J. Wei X. Pei Y. Li X. Si G. Chen X.Y. Chen Z.S. Dong Y. Zou F. Shi W. Qiu Q. Qian H. Liu G. J. Med. Chem. 2020 63 10 5458 5476 10.1021/acs.jmedchem.0c00337 32329342
    [Google Scholar]
24. Kim D. Hong S. Org. Lett. 2011 13 16 4466 4469 10.1021/ol2018278 21797199
    [Google Scholar]
25. Kim Y. Moon Y. Kang D. Hong S. Org. Biomol. Chem. 2014 12 21 3413 3422 10.1039/C4OB00180J 24740372
    [Google Scholar]