L-proline/cholesterol and diosgenin based thiourea cooperative system for the direct asymmetric aldol reaction in the presence of water

L-proline/cholesterol and diosgenin based thiourea cooperative system for the direct asymmetric aldol reaction in the presence of water

A series of cholesterol and based hydrophobic urea and thiourea compounds were synthesized and successfully used as a cocatalyst for L-proline catalyzed aldol reactions in the presence of water. The anticonfigured products were obtained with good yields (up to 94%), high diastereoselectivities (up to 95:5), and high enantiomeric excesses (up to 93% ee). The successful results for catalytic efficiency of L-proline in the presence of water reveal the importance of the hydrophobic nature of cholesterol and diosgenin parts of thiourea on the reactivity and selectivity in the presence of water.

___

  • 1. Mahrwald R. Modern Methods in Stereoselective Aldol Reactions. Weinheim, Germany: Wiley-VCH, 2013.
  • 2. Trost BM, Brindle CS. The direct catalytic asymmetric aldol reaction. Chemical Society Reviews 2010; 39 (5): 1600-1632.
  • 3. Yamashita Y, Yasukawa T, YooWJ, Kitanosono T, Kobayashi S. Catalytic enantioselective aldol reactions. Chemical Society Reviews 2018; 47 (12): 4388-4480.
  • 4. List B, Lerner RA, Barbas CF. Proline-catalyzed direct asymmetric aldol reactions. Journal of the American Chemical Society 2000; 122(10): 2395-2396.
  • 5. Anebouselvy K, Shruthi KS, Ramachary DB. Asymmetric supramolecular organocatalysis: a complementary upgrade to organocatalysis. European Journal of Organic Chemistry 2017; 37: 5460-5483.
  • 6. Hong L, Sun W, Yang D, Li G, Wang R. Additive effects on asymmetric catalysis. Chemical Reviews 2016; 116: 4006-4123.
  • 7. Reis O, Eymur S, Reis B, Demir AS. Direct enantioselective aldol reactions catalyzed by a proline-thiourea host-guest complex. Chemical Communications 2009 (9): 1088-1090.
  • 8. Amedjkouh M. Primary amine catalyzed direct asymmetric aldol reaction assisted by water. Tetrahedron-Asymmetry 2005; 16 (8): 1411- 1414.
  • 9. Nyberg AI, Usano A, Pihko PM. Proline-catalyzed ketone-aldehyde aldol reactions are accelerated by water. Synlett 2004 (11): 1891-1896.
  • 10. Pihko PM, Laurikainen KM, Usano A, Nyberg AI, Kaavi JA. Effect of additives on the proline-catalyzed ketone-aldehyde aldol reactions. Tetrahedron 2006; 62 (2-3): 317-328.
  • 11. Zhou Y, Shan ZX. Chiral diols: A new class of additives for direct aldol reaction catalyzed by L-proline. Journal of Organic Chemistry 2006; 71 (25): 9510-9512.
  • 12. Zhou Y, Shan ZX. (R)- or (S)-bi-2-naphthol assisted, L-proline catalyzed direct aldol reaction. Tetrahedron-Asymmetry 2006; 17 (11): 1671-1677.
  • 13. Companyó X, Valero G, Crovetto L, Moyano A, Rios R. Highly enantio- and diastereoselective organocatalytic desymmetrization of prochiral cyclohexanones by simple direct aldol reaction catalyzed by proline. Chemistry – A European Journal 2009; 15 (27): 6564-6568.
  • 14. El-Hamdouni N, Companyó X, Rios R, Moyano A. Substrate-dependent nonlinear effects in proline–thiourea-catalyzed aldol reactions: unraveling the role of the thiourea co-catalyst. Chemistry – A European Journal 2010; 16 (4): 1142-1148.
  • 15. Demircan E, Eymur S, Demir AS. Proline-calixarene thiourea host-guest complex catalyzed enantioselective aldol reactions: from nonpolar solvents to the presence of water. Tetrahedron-Asymmetry 2014; 25 (5): 443-448.
  • 16. Demir AS, Basceken S. Self-assembly of an organocatalyst for the enantioselective synthesis of Michael adducts and alpha-aminoxy alcohols in a nonpolar medium. Tetrahedron-Asymmetry 2013; 24 (19): 1218-1224.
  • 17. Demir AS, Basceken S. Synthesis of a bipyridine-derived achiral thiourea trifluoromethanesulfonic acid salt and its application as an additive in organocatalytic asymmetric reactions. Tetrahedron Letters 2013; 54 (42): 5677-5681.
  • 18. Cho E, Kim TH. Direct asymmetric aldol reaction co-catalyzed by L-proline and isothiouronium salts. Tetrahedron Letters 2014; 55 (47): 6470-6473.
  • 19. Porcar R, Ríos-Lombardía N, Busto E, Gotor-Fernández V, Gotor V et al. Chemoenzymatic synthesis of optically active 2-(2′- or 4′-substituted-1H-imidazol-1-yl)cycloalkanols: chiral additives for (l)-proline. Catalysis Science & Technology 2013; 3 (10): 2596-2601.
  • 20. Martínez-Castañeda Á, Poladura B, Rodríguez-Solla H, Concellón C, del Amo V. Direct aldol reactions catalyzed by a heterogeneous guanidinium salt/proline system under solvent-free conditions. Organic Letters 2011; 13 (12): 3032-3035.
  • 21. Bhowmick S, Bhowmick KC. Catalytic asymmetric carbon-carbon bond-forming reactions in aqueous media. Tetrahedron-Asymmetry 2011; 22 (23): 1945-1979.
  • 22. Li C-J. Organic reactions in aqueous media with a focus on carbon−carbon bond formations: a decade update. Chemical Reviews 2005; 105 (8): 3095-3166.
  • 23. Isart C, Bures J, Vilarrasa J. Seebach’s oxazolidinone is a good catalyst for aldol reactions. Tetrahedron Letters 2008; 49 (37): 5414-5418.
  • 24. List B, Hoang L, Martin HJ. New mechanistic studies on the proline-catalyzed aldol reaction. In: Proceedings of the National Academy of Sciences of the United States of America 2004; 101 (16): 5839-5842.
  • 25. Hayashi Y, Aratake S, Okano T, Takahashi J, Sumiya T et al. Combined proline–surfactant organocatalyst for the highly diastereo- and enantioselective aqueous direct cross-aldol reaction of aldehydes. Angewandte Chemie International Edition 2006; 45 (33): 5527-5529.
  • 26. Hayashi Y, Sumiya T, Takahashi J, Gotoh H, Urushima T et al. Highly diastereo- and enantioselective direct aldol reactions in water. Angewandte Chemie International Edition 2006; 45 (6): 958-961.
  • 27. Mase N, Nakai Y, Ohara N, Yoda H, Takabe K et al. Organocatalytic direct asymmetric aldol reactions in water. Journal of the American Chemical Society 2006; 128 (3): 734-735.
  • 28. Mase N, Watanabe K, Yoda H, Takabe K, Tanaka F et al. Organocatalytic direct michael reaction of ketones and aldehydes with β-nitrostyrene in brine. Journal of the American Chemical Society 2006; 128 (15): 4966-4967.
  • 29. Giacalone F, Gruttadauria F. Water in Organocatalytic Reactions. In: Dalko PI (editor). Comprehensive Enantioselective Organocatalysis. Weinheim, Germany: Wiley-VCH, 2013, pp. 673-717.
  • 30. Bhowmick S, Mondal A, Ghosh ABhowmick K C. Water: the most versatile and nature’s friendly media in asymmetric organocatalyzed direct aldol reactions. Tetrahedron-Asymmetry 2015; 26 (21-22): 1215-1244.
  • 31. Jimeno C. Water in asymmetric organocatalytic systems: a global perspective. Organic & Biomolecular Chemistry 2016; 14 (26): 6147- 6164.
  • 32. van der Helm MP, Klemm B, Eelkema R. Organocatalysis in aqueous media. Nature Reviews Chemistry 2019; 3 (8): 491-508.
  • 33. He T, Li K, Wu MY, Wu MB, Wang N et al. Water promoted enantioselective aldol reaction by proline-cholesterol and -diosgenin based amphiphilic organocatalysts. Tetrahedron 2013; 69 (25): 5136-5143.
  • 34. Jana A, Ikbal M, Singh NDP. Perylen-3-ylmethyl: fluorescent photoremovable protecting group (FPRPG) for carboxylic acids and alcohols. Tetrahedron 2012; 68 (4): 1128-1136.
  • 35. Chen FB, Huang S, Zhang H, Liu FY, Peng YG. Proline-based dipeptides with two amide units as organocatalyst for the asymmetric aldol reaction of cyclohexanone with aldehydes. Tetrahedron 2008; 64 (40): 9585-9591.
  • 36. D’Elia V, Zwicknagl H, Reiser O. Short α/β-peptides as catalysts for intra- and intermolecular aldol reactions. The Journal of Organic Chemistry 2008; 73 (8): 3262-3265.
  • 37. Maya V, Raj M, Singh VK. Highly enantioselective organocatalytic direct aldol reaction in an aqueous medium. Organic Letters 2007; 9 (13): 2593-2595.
  • 38. Fu SD, Fu XK, Zhang SP, Zou XC, Wu XJ. Highly diastereo- and enantioselective direct aldol reactions by 4-tert-butyldimethylsiloxysubstituted organocatalysts derived from N-prolylsulfonamides in water. Tetrahedron-Asymmetry 2009; 20 (20): 2390-2396.
  • 39. Tang Z, Yang Z-H, Chen X-H, Cun L-F, Mi A-Q et al. A highly efficient organocatalyst for direct aldol reactions of ketones with aldedydes. Journal of the American Chemical Society 2005; 127 (25): 9285-9289.