Abstract:
A new solvent-free procedure for C–O cross-coupling between phenols and aryl bromides comprising of Pd2(dba)3/ButBrettPhos catalytic system is efficient for substrates bearing donor or acceptor, as well as bulky substituents.
Citation:
S. A. Rzhevskiy, M. A. Topchiy, V. N. Bogachev, L. I. Minaeva, I. R. Cherkashchenko, K. V. Lavrov, G. K. Sterligov, M. S. Nechaev, A. F. Asachenko, “Solvent-free palladium-catalyzed C–O cross-coupling of aryl bromides with phenols”, Mendeleev Commun., 31:3 (2021), 409–411
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https://www.mathnet.ru/eng/mendc946
https://www.mathnet.ru/eng/mendc/v31/i3/p409
This publication is cited in the following 8 articles:
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Y. Zhou, Ya.-J. Fan, L. Wang, “β-Cyclodextrin-stabilized Cu nanoparticles catalyzed C–O coupling to access 2-aryloxypyridines”, Mendeleev Commun., 34:2 (2024), 270–271
T. S. Sukhikh, M. P. Davydova, A. V. Artem'ev, “Crystal structure of tetrakis(triphenylphosphine)palladium(0)”, Mendeleev Commun., 33:2 (2023), 171–173
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A. A. Vasil'ev, A. S. Burukin, G. M. Zhdankina, S. G. Zlotin, “Functionalized polychloroarenes in the Bichwald ligand-promoted Suzuki cross-coupling”, Russ Chem Bull, 71:8 (2022), 1656
Olga V. Shurupova, Sergey A. Rzhevskiy, Lidiya I. Minaeva, Maxim A. Topchiy, Andrey F. Asachenko, “Highly efficient synthesis of 3,4-diarylbutadiene sulfones using Heck–Matsuda reaction”, RSC Adv., 12:9 (2022), 5517
O. V. Shurupova, G. K. Sterligov, M. A. Rasskazova, E. A. Drokin, A. N. Lysenko, S. A. Rzhevskiy, L. I. Minaeva, M. A. Topchiy, A. F. Asachenko, “One-pot two step synthesis of unsymmetrically substituted indenes from 3,4-diarylbutadiene sulfones”, Mendeleev Commun., 32:4 (2022), 446–448