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158 related items for PubMed ID: 33764064

  • 21. Oxazole as an electron-deficient diene in the Diels-Alder reaction.
    Suárez-Moreno GV, González-Zamora E, Méndez F.
    Org Lett; 2011 Dec 16; 13(24):6358-61. PubMed ID: 22074462
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  • 22. Origin of asynchronicity in Diels-Alder reactions.
    Vermeeren P, Hamlin TA, Bickelhaupt FM.
    Phys Chem Chem Phys; 2021 Sep 22; 23(36):20095-20106. PubMed ID: 34499069
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  • 23. Enantiodivergent [4+2] Cycloaddition of Dienolates by Polyfunctional Lewis Acid/Zwitterion Catalysis.
    Miskov-Pajic V, Willig F, Wanner DM, Frey W, Peters R.
    Angew Chem Int Ed Engl; 2020 Nov 02; 59(45):19873-19877. PubMed ID: 32697020
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  • 24. Mukaiyama aldol reaction catalyzed by (benz)imidazolium-based halogen bond donors.
    Sutar RL, Erochok N, Huber SM.
    Org Biomol Chem; 2021 Jan 28; 19(4):770-774. PubMed ID: 33432958
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  • 25. Insights into the Diels-Alder Reaction between 3-Vinylindoles and Methyleneindolinone without and with the Assistance of Hydrogen-Bonding Catalyst Bisthiourea: Mechanism, Origin of Stereoselectivity, and Role of Catalyst.
    Yan CX, Yang F, Yang X, Zhou DG, Zhou PP.
    J Org Chem; 2017 Mar 17; 82(6):3046-3061. PubMed ID: 28225628
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  • 26. A new approach to promoting sluggish Diels-Alder reactions: dihapto-coordination of the diene.
    Liu W, You F, Mocella CJ, Harman WD.
    J Am Chem Soc; 2006 Feb 08; 128(5):1426-7. PubMed ID: 16448094
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  • 27. Computational Design of Bidentate Hypervalent Iodine Catalysts in Halogen Bond-Mediated Organocatalysis.
    O'Brien J, Melnyk N, Lee RS, James M, Trujillo C.
    Chemphyschem; 2024 Nov 18; 25(22):e202400515. PubMed ID: 38973286
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  • 28. Iodine(I)-based and iodine(III)-based halogen bond catalysis on the Friedel-Crafts reaction: a theoretical study.
    Zhao C, Li Y, Li X, Zeng Y.
    Phys Chem Chem Phys; 2023 Aug 09; 25(31):21100-21108. PubMed ID: 37527332
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  • 29. Bis-Boron Compounds in Catalysis: Bidentate and Bifunctional Activation.
    Schweighauser L, Wegner HA.
    Chemistry; 2016 Sep 26; 22(40):14094-103. PubMed ID: 27490466
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  • 30. Impact of C=C/B-N Replacement on the Diels-Alder Reactivity of Curved Polycyclic Aromatic Hydrocarbons.
    García-Rodeja Y, Fernández I.
    Chemistry; 2019 Jul 22; 25(41):9771-9779. PubMed ID: 31149750
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  • 31. Catalysis of a Diels-Alder Reaction by Amidinium Ions.
    Schuster T, Kurz M, Göbel MW.
    J Org Chem; 2000 Mar 24; 65(6):1697-1701. PubMed ID: 10814142
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  • 32. Quantum chemical study of Diels-Alder reactions catalyzed by Lewis acid activated oxazaborolidines.
    Sakata K, Fujimoto H.
    J Org Chem; 2013 Apr 05; 78(7):3095-103. PubMed ID: 23373629
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  • 33. Kinetic study of the Diels-Alder reaction of Li⁺@C₆₀ with cyclohexadiene: greatly increased reaction rate by encapsulated Li⁺.
    Ueno H, Kawakami H, Nakagawa K, Okada H, Ikuma N, Aoyagi S, Kokubo K, Matsuo Y, Oshima T.
    J Am Chem Soc; 2014 Aug 06; 136(31):11162-7. PubMed ID: 25006694
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  • 34. Domino inverse electron-demand Diels-Alder/cyclopropanation reaction of diazines catalyzed by a bidentate Lewis acid.
    Kessler SN, Neuburger M, Wegner HA.
    J Am Chem Soc; 2012 Oct 31; 134(43):17885-8. PubMed ID: 23066957
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  • 35. Thiourea-catalyzed Diels-Alder reaction of a naphthoquinone monoketal dienophile.
    Kramer CS, Bräse S.
    Beilstein J Org Chem; 2013 Oct 31; 9():1414-8. PubMed ID: 23946836
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  • 36. 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
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  • 37. DFT Study of Solvent Effects in Acid-Catalyzed Diels-Alder Cycloadditions of 2,5-Dimethylfuran and Maleic Anhydride.
    Salavati-fard T, Caratzoulas S, Doren DJ.
    J Phys Chem A; 2015 Sep 24; 119(38):9834-43. PubMed ID: 26331220
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  • 38. Origins of stereoselectivity in uncatalyzed and ZnBr2-catalyzed Diels-Alder reactions of a chiral sulfinylquinone.
    Chow KH, Krenske EH.
    Org Biomol Chem; 2019 Oct 14; 17(38):8756-8767. PubMed ID: 31553037
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  • 39. A computational investigation of the selectivity and mechanism of the Lewis acid catalyzed oxa-Diels-Alder cycloaddition of substituted diene with benzaldehyde.
    Khorief Nacereddine A, Merzoud L, Morell C, Chermette H.
    J Comput Chem; 2021 Jul 05; 42(18):1296-1311. PubMed ID: 33931864
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  • 40. Asymmetric Synthesis of Hydrocarbazoles Catalyzed by an Octahedral Chiral-at-Rhodium Lewis Acid.
    Huang Y, Song L, Gong L, Meggers E.
    Chem Asian J; 2015 Dec 05; 10(12):2738-43. PubMed ID: 26344422
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