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Journal Abstract Search

374 related items for PubMed ID: 24375806

  • 21. 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]

  • 22. Exo-Selective Diels-Alder Reactions.
    Li YH, Chen JH, Yang Z.
    Chemistry; 2024 Mar 20; 30(17):e202304371. PubMed ID: 38412422
    [Abstract] [Full Text] [Related]

  • 23. 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]

  • 24. Synthesis of endo-fused 5-unsubstituted Hexahydro-2H-pyrano[3,2-c]quinolinesvia Sequential Sc(OTf)3-catalyzed Cationic Imino-Diels-Alder Reaction/N-debenzylation using N-benzylanilines, 3,4-dihydro-2H-pyran and Paraformaldehyde under MW Irradiation.
    Salgado ARM, Galvis CEP, Kouznetsov VV, Meléndez CM.
    Curr Org Synth; 2021 Jan 06; 18(5):431-442. PubMed ID: 33441074
    [Abstract] [Full Text] [Related]

  • 25. Hydroxyapatite-bound cationic ruthenium complexes as novel heterogeneous lewis acid catalysts for Diels-Alder and aldol reactions.
    Mori K, Hara T, Mizugaki T, Ebitani K, Kaneda K.
    J Am Chem Soc; 2003 Sep 24; 125(38):11460-1. PubMed ID: 13129324
    [Abstract] [Full Text] [Related]

  • 26. 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]

  • 27. FeCl3 as an Ion-Pairing Lewis Acid Catalyst. Formation of Highly Lewis Acidic FeCl2+ and Thermodynamically Stable FeCl4- To Catalyze the Aza-Diels-Alder Reaction with High Turnover Frequency.
    Tomifuji R, Maeda K, Takahashi T, Kurahashi T, Matsubara S.
    Org Lett; 2018 Dec 07; 20(23):7474-7477. PubMed ID: 30427692
    [Abstract] [Full Text] [Related]

  • 28. Why do five-membered heterocyclic compounds sometimes not participate in polar Diels-Alder reactions?
    Domingo LR, Pérez P, Ortega DE.
    J Org Chem; 2013 Mar 15; 78(6):2462-71. PubMed ID: 23350936
    [Abstract] [Full Text] [Related]

  • 29. Chiral Supramolecular U-Shaped Catalysts Induce the Multiselective Diels-Alder Reaction of Propargyl Aldehyde.
    Hatano M, Sakamoto T, Mizuno T, Goto Y, Ishihara K.
    J Am Chem Soc; 2018 Nov 28; 140(47):16253-16263. PubMed ID: 30404439
    [Abstract] [Full Text] [Related]

  • 30. Mechanisms and Origins of Selectivities of the Lewis Acid-Catalyzed Diels-Alder Reactions between Arylallenes and Acrylates.
    Yu P, Li W, Houk KN.
    J Org Chem; 2017 Jun 16; 82(12):6398-6402. PubMed ID: 28510451
    [Abstract] [Full Text] [Related]

  • 31. Tandem enyne metathesis-Diels-Alder reaction for construction of natural product frameworks.
    Rosillo M, Domínguez G, Casarrubios L, Amador U, Pérez-Castells J.
    J Org Chem; 2004 Mar 19; 69(6):2084-93. PubMed ID: 15058956
    [Abstract] [Full Text] [Related]

  • 32. DNA-based hybrid catalysts for asymmetric organic synthesis.
    Park S, Sugiyama H.
    Angew Chem Int Ed Engl; 2010 May 25; 49(23):3870-8. PubMed ID: 20455226
    [Abstract] [Full Text] [Related]

  • 33. Synthesis of highly substituted cyclohexenes via mixed Lewis acid-catalyzed Diels-Alder reactions of highly substituted dienes and dienophiles.
    Jung ME, Ho D, Chu HV.
    Org Lett; 2005 Apr 14; 7(8):1649-51. PubMed ID: 15816774
    [Abstract] [Full Text] [Related]

  • 34. Low-oxidation state indium-catalyzed C-C bond formation.
    Schneider U, Kobayashi S.
    Acc Chem Res; 2012 Aug 21; 45(8):1331-44. PubMed ID: 22626010
    [Abstract] [Full Text] [Related]

  • 35. Direct organocatalytic asymmetric heterodomino reactions: the Knoevenagel/Diels-Alder/epimerization sequence for the highly diastereoselective synthesis of symmetrical and nonsymmetrical synthons of benzoannelated centropolyquinanes.
    Ramachary DB, Anebouselvy K, Chowdari NS, Barbas CF.
    J Org Chem; 2004 Sep 03; 69(18):5838-49. PubMed ID: 15373469
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  • 36. The diarylprolinol silyl ether system: a general organocatalyst.
    Jensen KL, Dickmeiss G, Jiang H, Albrecht L, Jørgensen KA.
    Acc Chem Res; 2012 Feb 21; 45(2):248-64. PubMed ID: 21848275
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  • 37. Catalysis of a Diels-Alder Reaction between Azachalcones and Cyclopentadiene by a Recyclable Copper(II)-PEIP Metal-Organic Framework.
    Hadjikyprianou E, Petrides S, Kourtellaris A, Tasiopoulos AJ, Georgiades SN.
    Materials (Basel); 2023 Jul 27; 16(15):. PubMed ID: 37570002
    [Abstract] [Full Text] [Related]

  • 38. B(C6F5)3: A New Class of Strong and Bulky Lewis Acid for Exo-Selective Intermolecular Diels-Alder Reactions of Unreactive Acyclic Dienes with α,β-Enals.
    Zhou JH, Jiang B, Meng FF, Xu YH, Loh TP.
    Org Lett; 2015 Sep 18; 17(18):4432-5. PubMed ID: 26351987
    [Abstract] [Full Text] [Related]

  • 39. DFT investigation of solvent, substituent, and catalysis effects on the intramolecular Diels-Alder reaction.
    Gara R, Zouaghi MO, ALshandoudi LMH, Arfaoui Y.
    J Mol Model; 2021 Apr 07; 27(5):125. PubMed ID: 33829417
    [Abstract] [Full Text] [Related]

  • 40. Effect of Lewis acid catalysts on Diels-Alder and hetero-Diels-Alder cycloadditions sharing a common transition state.
    Celebi-Olçüm N, Ess DH, Aviyente V, Houk KN.
    J Org Chem; 2008 Oct 03; 73(19):7472-80. PubMed ID: 18781801
    [Abstract] [Full Text] [Related]

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