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Mendeleev Communications, 2011, Volume 21, Issue 1, Pages 1–3
DOI: https://doi.org/10.1016/j.mencom.2011.01.001
(Mi mendc2844)
 

This article is cited in 10 scientific papers (total in 10 papers)

Diastereoselectivity of allylboration of aromatic aldehydes with 1,6-bis(dipropylboryl)hexa-2,4-diene

A. N. Anfimova, S. Yu. Erdyakova, M. E. Gurskiia, A. V. Ignatenkoa, K. A. Lyssenkob, Yu. N. Bubnovab

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Allylboration of aromatic aldehydes with 1,6-bis(dipropylboryl)hexa-2,4-diene stereoselectively furnishes only two diastereomeric 1,4-diaryl-2,3-divinyl-1,4-diols with threo-configuration at C(2) and C(3).
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (110.1 Kb)


Citation: A. N. Anfimov, S. Yu. Erdyakov, M. E. Gurskii, A. V. Ignatenko, K. A. Lyssenko, Yu. N. Bubnov, “Diastereoselectivity of allylboration of aromatic aldehydes with 1,6-bis(dipropylboryl)hexa-2,4-diene”, Mendeleev Commun., 21:1 (2011), 1–3
Linking options:
  • https://www.mathnet.ru/eng/mendc2844
  • https://www.mathnet.ru/eng/mendc/v21/i1/p1
  • This publication is cited in the following 10 articles:
    1. Ming Bao, Michael P. Doyle, “Asymmetric [3+n]‐Cycloaddition Reactions of Donor‐Acceptor Cyclopropanes”, ChemCatChem, 15:23 (2023)  crossref
    2. M. E. Gursky, S. V. Baranin, K. A. Lyssenko, O. O. Chudakova, Yu. N. Bubnov, “Total synthesis of diaeudesmin and epieudesmin enantiomers from diallyl”, Russ Chem Bull, 71:8 (2022), 1729  crossref
    3. M. E. Gurskii, M. I. Zuev, A. V. Eshtukov, D. A. Cheshkov, S. V. Baranin, Yu. N. Bubnov, “Stereospecific synthesis of aryltetraline lignan analogues using 1,6-bis(dipropylboryl)hexa-2,4-diene”, Mendeleev Commun., 31:5 (2021), 693–695  mathnet  crossref
    4. Ranadeep Talukdar, “Synthetically important ring opening reactions by alkoxybenzenes and alkoxynaphthalenes”, RSC Adv., 10:52 (2020), 31363  crossref
    5. Belinda E. Hetzler, Giulio Volpin, Elisa Vignoni, Ana G. Petrovic, Gloria Proni, Chunhua T. Hu, Dirk Trauner, “Ein vielseitiges Bisallylbor‐Reagenz für die stereoselektive Synthese von chiralen Diolen”, Angewandte Chemie, 130:43 (2018), 14472  crossref
    6. Belinda E. Hetzler, Giulio Volpin, Elisa Vignoni, Ana G. Petrovic, Gloria Proni, Chunhua T. Hu, Dirk Trauner, “A Versatile Bis‐Allylboron Reagent for the Stereoselective Synthesis of Chiral Diols”, Angew Chem Int Ed, 57:43 (2018), 14276  crossref
    7. B. A. Murray, Organic Reaction Mechanisms Series, Organic Reaction Mechanisms 2011, 2014, 1  crossref
    8. P.V. Ramachandran, P.D. Gagare, D.R. Nicponski, Comprehensive Organic Synthesis II, 2014, 1  crossref
    9. A. N. Anfimov, S. Yu. Erdyakov, M. E. Gurskii, Yu. N. Bubnov, “Stereospecific synthesis of endo-endo-3,7-dioxabicyclo[3.3.0]octane lignans using 1,6-bis(dipropylboryl)-2,4-hexadiene”, Russ Chem Bull, 60:11 (2011), 2336  crossref
    10. Alexander N. Anfimov, Sergey Yu. Erdyakov, Mikhail E. Gurskii, Anatolii V. Ignatenko, Konstantin A. Lyssenko, Yurii N. Bubnov, “ChemInform Abstract: Diastereoselectivity of Allylboration of Aromatic Aldehydes with 1,6‐Bis(dipropylboryl)hexa‐2,4‐diene.”, ChemInform, 42:26 (2011)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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