Abstract:
A direct asymmetric aldol reaction between unmodified ketones and aldehydes was achieved for the first time using the 1(R),2(R)-bis[(S)-prolinamido]cyclohexane/[bmim][BF4] ionic liquid catalytic system.
Document Type:
Article
Language: English
Citation:
A. S. Kucherenko, D. E. Siyutkin, V. O. Muraviev, M. I. Struchkova, S. G. Zlotin, “1(R),2(R)-Bis[(S)-prolinamido]cyclohexane/[bmim][BF4] ionic liquid as an efficient catalytic system for direct asymmetric aldol reactions”, Mendeleev Commun., 17:5 (2007), 277–278
Linking options:
https://www.mathnet.ru/eng/mendc3456
https://www.mathnet.ru/eng/mendc/v17/i5/p277
This publication is cited in the following 14 articles:
Elena S. Filatova, Olga V. Fedorova, Irina G. Ovchinnikova, Sergei V. Kochetkov, Konstantin A. Chistiakov, Gennady L. Rusinov, “Asymmetric Synthesis of Dihydropyrimidinethione Podand in the Presence of C2‐Symmetric Bis(Hydroxy)Proline‐Containing Amides”, ChemistrySelect, 9:17 (2024)
Akash Mishra, Stephen Hanessian, “1,2-trans-Diaminocyclohexane (DACH) in Asymmetric Catalysis: Nearing Fifty Years of Faithful Service and Counting”, Synthesis, 56:18 (2024), 2747
Jeffrey S. Price, David J.H. Emslie, Comprehensive Organometallic Chemistry IV, 2022, 378
S. G. Zlotin, S. V. Kochetkov, “C2-symmetric diamines and their derivatives as promising organocatalysts for asymmetric synthesis”, Russian Chem. Reviews, 84:11 (2015), 1077–1099
Ling-yan Liu, Bing Wang, Yunna Zhu, Wei-xing Chang, Jing Li, “Additive-controlled regioselective direct asymmetric aldol reaction of hydroxyacetone and aldehyde”, Tetrahedron: Asymmetry, 24:9-10 (2013), 533
Dmitry E. Siyutkin, Alexander S. Kucherenko, Sergei G. Zlotin, Comprehensive Enantioselective Organocatalysis, 2013, 617
A. S. Kucherenko, D. E. Siyutkin, O. V. Maltsev, S. V. Kochetkov, S. G. Zlotin, “Asymmetric organocatalysis: from proline to highly efficient immobilized organocatalysts”, Russ Chem Bull, 61:7 (2012), 1313
Štefan Toma, Radovan Šebesta, Ionic Liquids in Biotransformations and Organocatalysis, 2012, 331
Long Zhang, Sanzhong Luo, Jin-Pei Cheng, “Non-covalent immobilization of asymmetric organocatalysts”, Catal. Sci. Technol., 1:4 (2011), 507
Dmitry E. Siyutkin, Alexander S. Kucherenko, Sergei G. Zlotin, “A new (S)-prolinamide modified by an ionic liquid moiety—a high performance recoverable catalyst for asymmetric aldol reactions in aqueous media”, Tetrahedron, 66:2 (2010), 513
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
Alexandre F. Trindade, Pedro M. P. Gois, Carlos A. M. Afonso, “Recyclable Stereoselective Catalysts”, Chem. Rev., 109:2 (2009), 418
Alexander S. Kucherenko, Dmitriy E. Siyutkin, Vladislav O. Muraviev, Marina I. Struchkova, Sergei G. Zlotin, “ChemInform Abstract: 1(R),2(R)‐Bis[(S)‐prolinamido]cyclohexane/[bmim][BF4] Ionic Liquid as an Efficient Catalytic System for Direct Asymmetric Aldol Reactions.”, ChemInform, 39:9 (2008)
A. S. Kucherenko, D. E. Syutkin, S. G. Zlotin, “Asymmetric aldol condensation in an ionic liquid-water system catalyzed by (S)-prolinamide derivatives.”, Russ Chem Bull, 57:3 (2008), 591
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