A Versatile Approach to Flavones Via a One-pot Pd(II)-catalyzed Dehydrogenation/oxidative Boron-Heck Coupling Sequence of Chromanones
Overview
Chemistry
Authors
Affiliations
A variety of flavones were expediently synthesized from readily accessible chromanones via a one-pot sequence involving Pd(II)-catalyzed dehydrogenation and oxidative boron-Heck coupling with arylboronic acid pinacol esters. In particular, the use of arylboronic acid pinacol esters was found to significantly improve the yield of the reaction.
Troshkova N, Politanskaya L, Wang J, Niukalova M, Khasanov S, Esaulkova I Mol Divers. 2024; 29(2):1427-1452.
PMID: 39012566 DOI: 10.1007/s11030-024-10925-6.
Radical-Induced Cascade Annulation/Hydrocarbonylation for Construction of 2-Aryl-4-chromen-4-ones.
He X, Xu K, Liu Y, Wang D, Tang Q, Hui W Molecules. 2022; 27(21).
PMID: 36364239 PMC: 9654733. DOI: 10.3390/molecules27217412.
Son S, Cho Y, Yoo H, Lee S, Kim Y, Jang H RSC Adv. 2022; 11(23):14000-14006.
PMID: 35423945 PMC: 8697754. DOI: 10.1039/d1ra01672e.
A novel one-pot synthesis of flavones.
Chang M, Tsai M, Lin C RSC Adv. 2022; 11(19):11655-11662.
PMID: 35423639 PMC: 8695955. DOI: 10.1039/d1ra00534k.
Synthesis of 2-Aryl-4-thiochromen-4-one Derivatives a Cross-Coupling Reaction.
Li P, Li S, Li G, Huang H ACS Omega. 2021; 6(22):14655-14663.
PMID: 34124488 PMC: 8190924. DOI: 10.1021/acsomega.1c01778.