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Mendeleev Communications, 2002, Volume 12, Issue 5, Pages 176–178
DOI: https://doi.org/10.1070/MC2002v012n05ABEH001623
(Mi mendc4150)
 

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

Synthesis of α,β-unsaturated esters from dialkoxyphosphoryl esters and aldehydes in the ionic liquid [bmim][PF6]

G. V. Kryshtal', G. M. Zhdankina, S. G. Zlotin

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Full-text PDF (89 kB) Citations (10)
Abstract: α,β-Unsaturated esters were synthesised by LiOH·H2O-promoted reactions of triethyl phosphonoacetate 1 and triethyl 3-methyl- 4-phosphono-2-butenoate 2 with aldehydes in 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]).
Document Type: Article
Language: English


Citation: G. V. Kryshtal', G. M. Zhdankina, S. G. Zlotin, “Synthesis of α,β-unsaturated esters from dialkoxyphosphoryl esters and aldehydes in the ionic liquid [bmim][PF6]”, Mendeleev Commun., 12:5 (2002), 176–178
Linking options:
  • https://www.mathnet.ru/eng/mendc4150
  • https://www.mathnet.ru/eng/mendc/v12/i5/p176
  • This publication is cited in the following 10 articles:
    1. Syed Rasheed, Devineni Subba Rao, Chennamsettty Subramanyam, Shaik Thaslim Basha, Chamarthi Naga Raju, “Expeditious, Nano-BF3 · SiO2-Catalyzed Michaelis–Arbuzov Reaction in an Ionic Liquid: Synthesis of Privileged Aryl/Heterocyclic Phosphonates”, Synthetic Communications, 44:20 (2014), 2988  crossref
    2. Venkat Reddy Chintareddy, Arkady Ellern, John G. Verkade, “P[N(i-Bu)CH2CH2]3N: Nonionic Lewis Base for Promoting the Room-Temperature Synthesis of α,β-Unsaturated Esters, Fluorides, Ketones, and Nitriles Using Wadsworth-Emmons Phosphonates”, J. Org. Chem., 75:21 (2010), 7166  crossref
    3. S. G. Zlotin, N. N. Makhova, “Ionic liquids as substrate-specific recoverable solvents and catalysts of regio-, stereo- and enantioselective organic reactions”, Mendeleev Commun., 20:2 (2010), 63–71  mathnet  crossref
    4. Oleg I. Artyushin, Daria V. Vorob'eva, Tamara P. Vasil'eva, Sergey N. Osipov, Gerd‐Volker Röschenthaler, Irina L. Odinets, “Facile synthesis of phosphorylated azides in ionic liquids and their use in the preparation of 1,2,3‐triazoles”, Heteroatom Chemistry, 19:3 (2008), 293  crossref
    5. Elena V. Sharova, Oleg I. Artyushin, Alexander S. Shaplov, Galina V. Myasoedova, Irina L. Odinets, “A novel facile synthesis of carbamoylmethylphosphine oxides in ionic liquids”, Tetrahedron Letters, 49:10 (2008), 1641  crossref
    6. I. L. Odinets, E. V. Matveeva, E. V. Sharova, O. I. Artyushin, V. A. Kozlov, D. V. Vorob'eva, S. N. Osipov, G. V. Röschenthaler, “Advantages of Organophosphorus Synthesis in Ionic Liquids: “Green” Approaches to Useful Phosphorus-Substituted Building Blocks”, Phosphorus, Sulfur, and Silicon and the Related Elements, 183:2-3 (2008), 383  crossref
    7. S. G. Zlotin, G. V. Kryshtal, G. M. Zhdankina, A. V. Bogolyubov, S. G. Postikova, V. A. Tartakovsky, “Synthesis of α-nitro derivatives of δ-oxocarboxylic and glutaric acids in heterogeneous catalytic system ionic liquid—KHCO3”, Russ Chem Bull, 56:8 (2007), 1487  crossref
    8. E.V. Matveeva, I.L. Odinets, V.A. Kozlov, A.S. Shaplov, T.A. Mastryukova, “Ionic-liquid-promoted Michaelis–Arbuzov rearrangement”, Tetrahedron Letters, 47:43 (2006), 7645  crossref
    9. Thies Thiemann, Masataka Watanabe, Yasuko Tanaka, Shuntaro Mataka, “Solvent-free Wittig olefination with stabilized phosphoranes—scope and limitations”, New J. Chem., 28:5 (2004), 578  crossref
    10. Galina V. Kryshtal, Galina M. Zhdankina, Sergei G. Zlotin, “Synthesis of α,β‐Unsaturated Esters from Dialkoxyphosphoryl Esters and Aldehydes in the Ionic Liquid [bmim][PF6]”, ChemInform, 34:13 (2003)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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