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Mendeleev Communications, 2010, Volume 20, Issue 2, Pages 63–71
DOI: https://doi.org/10.1016/j.mencom.2010.03.001
(Mi mendc2992)
 

This article is cited in 38 scientific papers (total in 38 papers)

Ionic liquids as substrate-specific recoverable solvents and catalysts of regio-, stereo- and enantioselective organic reactions

S. G. Zlotin, N. N. Makhova

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: The results obtained in the past few years concerning the use of ionic liquids and their congeners in reactions of organic compounds are summarized and the new opportunities opened by the use of such liquids instead of traditional organic solvents and catalysts are demonstrated.
Document Type: Article
Language: English


Citation: 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
Linking options:
  • https://www.mathnet.ru/eng/mendc2992
  • https://www.mathnet.ru/eng/mendc/v20/i2/p63
  • This publication is cited in the following 38 articles:
    1. Himani, Anirudh Pratap Singh Raman, Madhur Babu Singh, Pallavi Jain, Preeti Chaudhary, Indra Bahadur, Kashmiri Lal, Vinod Kumar, Prashant Singh, “An update on synthesis, properties, applications and toxicity of the ILs”, Journal of Molecular Liquids, 364 (2022), 119989  crossref
    2. Priya Ramasamy Shunmuga, Uma maheswari Govindhasamay, Deepa Manicam, Karthikeyan Parasuraman, “Imidazolium supported iron-chloroglycine complex, a good turnover recyclable catalyst for the solvent free synthesis of 3, 4-dihydropyrimidin-2(1H)-ones – promoted by ultrasound irradiation”, J. Mex. Chem. Soc., 62:3 (2019)  crossref
    3. Sergey A. Prikhod'ko, Anton Yu. Shabalin, Vadim V. Bardin, Ilia V. Eltsov, Inna K. Shundrina, Valentin N. Parmon, Nicolay Yu. Adonin, “1-Alkyl-3-methylimidazolium 4-organyloxy-2,3,5,6-tetrafluorophenyltrifluoroborates as a new platform for ionic liquids with specific properties”, RSC Adv., 7:28 (2017), 17497  crossref
    4. S. V. Kochetkov, A. S. Kucherenko, S. G. Zlotin, “Asymmetric Michael addition of aldehydes to maleimides in primary amine-based aqueous ionic liquid-supported recyclable catalytic system”, Mendeleev Commun., 27:5 (2017), 473–475  mathnet  crossref
    5. Nataliya P. Belskaya, Vasiliy A. Bakulev, Zhijin Fan, “Synthesis and (3+2) cycloaddition reactions of N,N ʹ- and C,N-cyclic azomethine imines”, Chem Heterocycl Comp, 52:9 (2016), 627  crossref
    6. L. L. Fershtat, D. V. Khakimov, N. N. Makhova, “Dinitrofuroxan cycloreversion as a novel general approach for the synthesis of nitroazoles”, Russ Chem Bull, 64:2 (2015), 415  crossref
    7. Mikhail I. Pleshchev, Nikita V. Das Gupta, Vladimir V. Kuznetsov, Ivan V. Fedyanin, Vadim V. Kachala, Nina N. Makhova, “CAN-mediated new, regioselective one-pot access to bicyclic cationic structures with 2,3-dihydro-1H-pyrazolo[1,2-a]pyrazol-4-ium core”, Tetrahedron, 71:47 (2015), 9012  crossref
    8. Carmen Nájera, José M. Sansano, Miguel Yus, “1,3-Dipolar cycloadditions of azomethine imines”, Org. Biomol. Chem., 13:32 (2015), 8596  crossref
    9. M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids”, Mendeleev Commun., 25:2 (2015), 126–128  mathnet  crossref
    10. M. I. Pleshchev, N. V. Das Gupta, M. I. Struchkova, A. S. Goloveshkin, I. S. Bushmarinov, D. V. Khakimov, N. N. Makhova, “Regio- and stereoselective cycloaddition of stable azomethine imines to (arylmethylidene)malononitriles”, Mendeleev Commun., 25:3 (2015), 188–190  mathnet  crossref
    11. L. L. Fershtat, S. S. Ashirbaev, A. S. Kulikov, V. V. Kachala, N. N. Makhova, “Ionic liquid-mediated synthesis of (1H-1,2,3-triazol-1-yl)furoxans by [3 + 2] cycloaddition of azidofuroxans to acetylenes”, Mendeleev Commun., 25:4 (2015), 257–259  mathnet  crossref
    12. M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Nucleophilic aromatic cine-substitution of hydrogen: the ionic liquid-promoted von Richter reaction”, Mendeleev Commun., 25:1 (2015), 41–43  mathnet  crossref
    13. Ilya V. Kuchurov, Albert G. Nigmatov, Evgeniya V. Kryuchkova, Alexey A. Kostenko, Alexandr S. Kucherenko, Sergei G. Zlotin, “Stereodivergent Michael addition of diphenylphosphite to α-nitroalkenes in the presence of squaramide-derived tertiary amines: an enantioselective organocatalytic reaction in supercritical carbon dioxide”, Green Chem., 16:3 (2014), 1521  crossref
    14. N. N. Makhova, M. I. Pleshchev, M. A. Epishina, A. S. Kulikov, “Synthesis and Transformations of Nitrogen Heterocycles in Ionic Liquids (Review)”, Chem Heterocycl Comp, 50:5 (2014), 634  crossref
    15. Alexander G. Zavozin, Nikolai V. Ignat'ev, Michael Schulte, Sergei G. Zlotin, “Synthesis of thiazole derivatives bearing an incorporated Z-5-aminopent-3-enoic acid fragment”, Tetrahedron, 69:34 (2013), 6975  crossref
    16. S. G. Zlotin, A. S. Kuherenko, O. V. Maltsev, A. O. Chizhov, “Chiral Ionic Liquid/ESI-MS Methodology as an Efficient Tool for the Study of Transformations of Supported Organocatalysts”, Top Catal, 56:11 (2013), 923  crossref
    17. Lyudmila F. Lourie, Yurii A. Serguchev, Maxim V. Ponomarenko, Eduard B. Rusanov, Michail V. Vovk, Nikolai V. Ignat'ev, “Electrophilic fluorocyclization of unsaturated alcohols in ionic liquids”, Tetrahedron, 69:2 (2013), 833  crossref
    18. Aleksei B. Sheremetev, Nataly S. Aleksandrova, Nadezhda V. Palysaeva, Marina I. Struchkova, Vladimir A. Tartakovsky, Kyrill Yu. Suponitsky, “Ionic Liquids as Unique Solvents in One‐Pot Synthesis of 4‐(N,2,2,2‐Tetranitroethylamino)‐3‐R‐Furazans”, Chemistry A European J, 19:37 (2013), 12446  crossref
    19. S. A. Prikhod'kv, N. Yu. Adonin, V. N. Parmon, “Activation of C-F bonds in ionic liquids catalyzed by nickel complex compounds”, Russ Chem Bull, 62:1 (2013), 33  crossref
    20. Dmitry E. Siyutkin, Alexander S. Kucherenko, Sergei G. Zlotin, Comprehensive Enantioselective Organocatalysis, 2013, 617  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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