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Journal Abstract Search

338 related items for PubMed ID: 14735517

  • 1. Evidence that protons can be the active catalysts in Lewis acid mediated hetero-Michael addition reactions.
    Wabnitz TC, Yu JQ, Spencer JB.
    Chemistry; 2004 Jan 23; 10(2):484-93. PubMed ID: 14735517
    [Abstract] [Full Text] [Related]

  • 2. A general, Brønsted acid-catalyzed hetero-Michael addition of nitrogen, oxygen, and sulfur nucleophiles.
    Wabnitz TC, Spencer JB.
    Org Lett; 2003 Jun 12; 5(12):2141-4. PubMed ID: 12790549
    [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
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  • 4. Investigation of Lewis acid versus Lewis base catalysis in asymmetric cyanohydrin synthesis.
    North M, Omedes-Pujol M, Williamson C.
    Chemistry; 2010 Oct 04; 16(37):11367-75. PubMed ID: 20715204
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  • 5. Acidic-functionalized ionic liquid as an efficient, green and reusable catalyst for hetero-Michael addition of nitrogen, sulfur and oxygen nucleophiles to α,β-unsaturated ketones.
    Han F, Yang L, Li Z, Xia C.
    Org Biomol Chem; 2012 Jan 14; 10(2):346-54. PubMed ID: 22076060
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  • 6. Heterogeneous versus homogeneous copper(II) catalysis in enantioselective conjugate-addition reactions of boron in water.
    Kitanosono T, Xu P, Kobayashi S.
    Chem Asian J; 2014 Jan 14; 9(1):179-88. PubMed ID: 24101583
    [Abstract] [Full Text] [Related]

  • 7. Lewis acid-Lewis acid heterobimetallic cooperative catalysis: mechanistic studies and application in enantioselective aza-Michael reaction.
    Yamagiwa N, Qin H, Matsunaga S, Shibasaki M.
    J Am Chem Soc; 2005 Sep 28; 127(38):13419-27. PubMed ID: 16173776
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  • 12. Enantioselective Carbonyl 1,2- or 1,4-Addition Reactions of Nucleophilic Silyl and Diazo Compounds Catalyzed by the Chiral Oxazaborolidinium Ion.
    Shim SY, Ryu DH.
    Acc Chem Res; 2019 Aug 20; 52(8):2349-2360. PubMed ID: 31314494
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  • 14. Octahedral Chiral-at-Metal Iridium Catalysts: Versatile Chiral Lewis Acids for Asymmetric Conjugate Additions.
    Shen X, Huo H, Wang C, Zhang B, Harms K, Meggers E.
    Chemistry; 2015 Jun 26; 21(27):9720-6. PubMed ID: 26033287
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  • 15. Development of atom-economical catalytic asymmetric reactions under proton transfer conditions: construction of tetrasubstituted stereogenic centers and their application to therapeutics.
    Kumagai N.
    Chem Pharm Bull (Tokyo); 2011 Jun 26; 59(1):1-22. PubMed ID: 21212541
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  • 16. Monomeric metal aqua complexes in the interlayer space of montmorillonites as strong Lewis acid catalysts for heterogeneous carbon-carbon bond-forming reactions.
    Kawabata T, Kato M, Mizugaki T, Ebitani K, Kaneda K.
    Chemistry; 2004 Dec 17; 11(1):288-97. PubMed ID: 15551316
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  • 17. From sigma- to pi-electrophilic Lewis acids. Application to selective organic transformations.
    Yamamoto Y.
    J Org Chem; 2007 Oct 12; 72(21):7817-31. PubMed ID: 17579452
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