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Mendeleev Communications, 2018, Volume 28, Issue 3, Pages 323–325
DOI: https://doi.org/10.1016/j.mencom.2018.05.032
(Mi mendc1753)
 

This article is cited in 7 scientific papers (total in 7 papers)

Communications

One-pot two-step stannylation/Stille homocoupling of aryl bromides and iodides under solvent-free conditions

P. S. Gribanovab, Yu. D. Golenkoa, M. A. Topchiyab, A. N. Philippovab, N. Yu. Kirilenkoab, N. V. Krivoshchapova, G. K. Sterligova, A. F. Asachenkoab, M. V. Bermeshevb, M. S. Nechaevab

a Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
b A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (204 kB) Citations (7)
Abstract: A new highly efficient solvent-free method for aryl bromide (iodide) homocoupling comprising the use of Pd(OAc)2/PCy3 system in the presence of CsF is suitable for substrates bearing functional groups not tolerant to lithium-, magnesium-, zincorganic reagents and strong bases.
Document Type: Article
Language: English


Citation: P. S. Gribanov, Yu. D. Golenko, M. A. Topchiy, A. N. Philippova, N. Yu. Kirilenko, N. V. Krivoshchapov, G. K. Sterligov, A. F. Asachenko, M. V. Bermeshev, M. S. Nechaev, “One-pot two-step stannylation/Stille homocoupling of aryl bromides and iodides under solvent-free conditions”, Mendeleev Commun., 28:3 (2018), 323–325
Linking options:
  • https://www.mathnet.ru/eng/mendc1753
  • https://www.mathnet.ru/eng/mendc/v28/i3/p323
  • This publication is cited in the following 7 articles:
    1. Xinchun Liu, Dan Zhang, Yanpeng Yuan, Jiawei Fu, Yuqing Kong, Yinyong Sun, “An unique method for the synthesis of ester compounds without the addition of solvent and catalyst”, Solid State Sciences, 149 (2024), 107468  crossref
    2. M. A. Topchiy, A. N. Lysenko, M. A. Rasskazova, A. A. Ageshina, S. A. Rzhevskiy, L. I. Minaeva, M. S. Nechaev, A. F. Asachenko, “Arylation of nitromethane with sterically hindered aryl halides”, Russ Chem Bull, 71:1 (2022), 59  crossref
    3. Pavel S. Gribanov, Edita M. Atoian, Anna N. Philippova, Maxim A. Topchiy, Andrey F. Asachenko, Sergey N. Osipov, “One‐Pot Synthesis of 5‐Amino‐1,2,3‐triazole Derivatives via Dipolar Azide-Nitrile Cycloaddition and Dimroth Rearrangement under Solvent‐Free Conditions”, Eur J Org Chem, 2021:9 (2021), 1378  crossref
    4. Sergey A. Rzhevskiy, Maxim A. Topchiy, Vasilii N. Bogachev, Lidiya I. Minaeva, Ilia R. Cherkashchenko, Konstantin V. Lavrov, Grigorii K. Sterligov, Mikhail S. Nechaev, Andrey F. Asachenko, “Solvent-free palladium-catalyzed C–O cross-coupling of aryl bromides with phenols”, Mendeleev Communications, 31:3 (2021), 409  crossref
    5. S. A. Rzhevskiy, V. N. Bogachev, L. I. Minaeva, G. K. Sterligov, M. S. Nechaev, M. A. Topchiy, A. F. Asachenko, “Efficient synthesis of 3-arylbutadiene sulfones using the Heck–Matsuda reaction”, Mendeleev Commun., 31:4 (2021), 548–549  mathnet  crossref
    6. G. A. Chesnokov, A. A. Ageshina, A. V. Maryanova, S. A. Rzhevskiy, P. S. Gribanov, M. A. Topchiy, M. S. Nechaev, A. F. Asachenko, “Nitromethane as a reagent for the synthesis of 3-nitroindoles from 2-haloarylamine derivatives”, Russ Chem Bull, 69:12 (2020), 2370  crossref
    7. P. S. Gribanov, G. A. Chesnokov, P. B. Dzhevakov, N. Yu. Kirilenko, S. A. Rzhevskiy, A. A. Ageshina, M. A. Topchiy, M. V. Bermeshev, A. F. Asachenko, M. S. Nechaev, “Solvent-free Suzuki and Stille cross-coupling reactions of 4- and 5-halo-1,2,3-triazoles”, Mendeleev Commun., 29:2 (2019), 147–149  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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