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Mendeleev Communications, 2021, Volume 31, Issue 3, Pages 409–411
DOI: https://doi.org/10.1016/j.mencom.2021.04.042
(Mi mendc946)
 

This article is cited in 8 scientific papers (total in 8 papers)

Communications

Solvent-free palladium-catalyzed C–O cross-coupling of aryl bromides with phenols

S. A. Rzhevskiyab, M. A. Topchiyab, V. N. Bogacheva, L. I. Minaevaa, I. R. Cherkashchenkoab, K. V. Lavrovc, G. K. Sterligova, M. S. Nechaevab, A. F. Asachenkoab

a A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, Russian Federation
b Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
c National Research Centre 'Kurchatov Institute', Moscow, Russian Federation
Full-text PDF (245 kB) Citations (8)
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.
Keywords: cross-coupling, phenols, arylation, solvent-free reactions, Pd-catalysis, aryl bromides, diaryl ethers.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.7 Mb)


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
Linking options:
  • https://www.mathnet.ru/eng/mendc946
  • https://www.mathnet.ru/eng/mendc/v31/i3/p409
  • This publication is cited in the following 8 articles:
    1. Olga V. Shurupova, Ekaterina S. Tarasova, Sergey A. Rzhevskiy, Lidiya I. Minaeva, Maxim A. Topchiy, Andrey F. Asachenko, “Novel convenient 2-step synthesis of pyrido[1,2-a]indoles from pyrylium salts and o-bromoanilines”, Org. Biomol. Chem., 22:33 (2024), 6742  crossref
    2. 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  mathnet  crossref
    3. T. S. Sukhikh, M. P. Davydova, A. V. Artem'ev, “Crystal structure of tetrakis(triphenylphosphine)palladium(0)”, Mendeleev Commun., 33:2 (2023), 171–173  mathnet  crossref
    4. G. K. Sterligov, A. N. Lysenko, E. A. Drokin, L. I. Minaeva, M. A. Topchiy, A. A. Ageshina, S. A. Rzhevskiy, M. S. Nechaev, A. F. Asachenko, “Solvent-free and transition metal catalyst-free synthesis of indolo[1,2-f]phenanthridine from 6-chlorophenanthridine”, Russ Chem Bull, 71:3 (2022), 479  crossref
    5. M. A. Topchiy, A. A. Ageshina, S. A. Rzhevskiy, L. I. Minaeva, M. S. Nechaev, A. F. Asachenko, “Solvent-free telomerization of isoprene with alcohols catalyzed by palladium(ɪɪ) carbene complexes”, Russ Chem Bull, 71:5 (2022), 940  crossref
    6. 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  crossref
    7. 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  crossref
    8. 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  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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