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195 related items for PubMed ID: 26917765

  • 1. Asymmetric Lewis acid organocatalysis of the Diels-Alder reaction by a silylated C-H acid.
    Gatzenmeier T, van Gemmeren M, Xie Y, Höfler D, Leutzsch M, List B.
    Science; 2016 Feb 26; 351(6276):949-52. PubMed ID: 26917765
    [Abstract] [Full Text] [Related]

  • 2. (1R)-(+)-camphor and acetone derived alpha'-hydroxy enones in asymmetric Diels-Alder reaction: catalytic activation by Lewis and Brønsted acids, substrate scope, applications in syntheses, and mechanistic studies.
    Bañuelos P, García JM, Gómez-Bengoa E, Herrero A, Odriozola JM, Oiarbide M, Palomo C, Razkin J.
    J Org Chem; 2010 Mar 05; 75(5):1458-73. PubMed ID: 20121243
    [Abstract] [Full Text] [Related]

  • 3. Silylium ion-catalyzed challenging Diels-Alder reactions: the danger of hidden proton catalysis with strong Lewis acids.
    Schmidt RK, Müther K, Mück-Lichtenfeld C, Grimme S, Oestreich M.
    J Am Chem Soc; 2012 Mar 07; 134(9):4421-8. PubMed ID: 22309027
    [Abstract] [Full Text] [Related]

  • 4. Stacking and Electrostatic Interactions Drive the Stereoselectivity of Silylium-Ion Asymmetric Counteranion-Directed Catalysis.
    Seguin TJ, Wheeler SE.
    Angew Chem Int Ed Engl; 2016 Dec 19; 55(51):15889-15893. PubMed ID: 27860103
    [Abstract] [Full Text] [Related]

  • 5. Aminocatalytic asymmetric Diels-Alder reactions via HOMO activation.
    Li JL, Liu TY, Chen YC.
    Acc Chem Res; 2012 Sep 18; 45(9):1491-500. PubMed ID: 22716926
    [Abstract] [Full Text] [Related]

  • 6. Brønsted-acid-catalyzed asymmetric multicomponent reactions for the facile synthesis of highly enantioenriched structurally diverse nitrogenous heterocycles.
    Yu J, Shi F, Gong LZ.
    Acc Chem Res; 2011 Nov 15; 44(11):1156-71. PubMed ID: 21800828
    [Abstract] [Full Text] [Related]

  • 7. Carbocations as Lewis acid catalysts in Diels-Alder and Michael addition reactions.
    Bah J, Franzén J.
    Chemistry; 2014 Jan 20; 20(4):1066-72. PubMed ID: 24375806
    [Abstract] [Full Text] [Related]

  • 8. Chiral Bimetallic Catalysts Derived from Chiral Metal Phosphates: Enantioselective Three-Component Asymmetric Aza-Diels-Alder Reactions of Cyclic Ketones.
    Deng Y, Karunaratne CV, Csatary E, Tierney DL, Wheeler K, Wang H.
    J Org Chem; 2015 Aug 21; 80(16):7984-93. PubMed ID: 26185962
    [Abstract] [Full Text] [Related]

  • 9. Chiral Dawson-Type Hybrid Polyoxometalate Catalyzes Enantioselective Diels-Alder Reactions.
    Xuan WJ, Botuha C, Hasenknopf B, Thorimbert S.
    Chemistry; 2015 Nov 09; 21(46):16512-6. PubMed ID: 26406341
    [Abstract] [Full Text] [Related]

  • 10. Orthogonal Catalysis for an Enantioselective Domino Inverse-Electron Demand Diels-Alder/Substitution Reaction.
    Beeck S, Ahles S, Wegner HA.
    Chemistry; 2022 Jan 24; 28(5):e202104085. PubMed ID: 34813113
    [Abstract] [Full Text] [Related]

  • 11. Unveiling the Delicate Balance of Steric and Dispersion Interactions in Organocatalysis Using High-Level Computational Methods.
    Yepes D, Neese F, List B, Bistoni G.
    J Am Chem Soc; 2020 Feb 19; 142(7):3613-3625. PubMed ID: 31984734
    [Abstract] [Full Text] [Related]

  • 12. Investigation of Lewis acid-catalyzed asymmetric aza-Diels-Alder reactions of 2H-azirines.
    Timén AS, Somfai P.
    J Org Chem; 2003 Dec 26; 68(26):9958-63. PubMed ID: 14682688
    [Abstract] [Full Text] [Related]

  • 13. Asymmetric Diels-Alder and inverse-electron-demand hetero-Diels-Alder reactions of β,γ-unsaturated α-ketoesters with cyclopentadiene catalyzed by N,N'-dioxide copper(II) complex.
    Zhu Y, Chen X, Xie M, Dong S, Qiao Z, Lin L, Liu X, Feng X.
    Chemistry; 2010 Oct 18; 16(39):11963-8. PubMed ID: 20827702
    [Abstract] [Full Text] [Related]

  • 14. Air-stable, storable, and highly efficient chiral zirconium catalysts for enantioselective Mannich-type, aza Diels-Alder, aldol, and hetero Diels-Alder reactions.
    Kobayashi S, Ueno M, Saito S, Mizuki Y, Ishitani H, Yamashita Y.
    Proc Natl Acad Sci U S A; 2004 Apr 13; 101(15):5476-81. PubMed ID: 15067139
    [Abstract] [Full Text] [Related]

  • 15. Design of an organocatalyst for the enantioselective Diels-Alder reaction with alpha-acyloxyacroleins.
    Ishihara K, Nakano K.
    J Am Chem Soc; 2005 Aug 03; 127(30):10504-5. PubMed ID: 16045334
    [Abstract] [Full Text] [Related]

  • 16. Oxathiaborolium: A Type of Chiral Lewis Acid Catalyst and Its Application in Catalytic and Highly Enantioselective Diels-Alder Reactions.
    Kumar SN, Yu IF, Chein RJ.
    Org Lett; 2017 Jan 06; 19(1):22-25. PubMed ID: 27981849
    [Abstract] [Full Text] [Related]

  • 17. Asymmetric Diels-Alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine.
    Corey EJ, Shibata T, Lee TW.
    J Am Chem Soc; 2002 Apr 17; 124(15):3808-9. PubMed ID: 11942799
    [Abstract] [Full Text] [Related]

  • 18. Brønsted-acid and Brønsted-base catalyzed Diels-Alder reactions.
    Shen J, Tan CH.
    Org Biomol Chem; 2008 Sep 21; 6(18):3229-36. PubMed ID: 18802626
    [Abstract] [Full Text] [Related]

  • 19. A new cationic, chiral catalyst for highly enantioselective Diels-Alder reactions.
    Sprott KT, Corey EJ.
    Org Lett; 2003 Jul 10; 5(14):2465-7. PubMed ID: 12841756
    [Abstract] [Full Text] [Related]

  • 20. Asymmetric Aza-Diels-Alder Reaction with Ion-Paired-Iron Lewis Acid-Brønsted Acid Catalyst.
    Tomifuji R, Kurahashi T, Matsubara S.
    Chemistry; 2019 Jul 05; 25(38):8987-8991. PubMed ID: 31066945
    [Abstract] [Full Text] [Related]

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