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Journal Abstract Search

167 related items for PubMed ID: 22452319

  • 1. Curtin-Hammett paradigm for stereocontrol in organocatalysis by diarylprolinol ether catalysts.
    Burés J, Armstrong A, Blackmond DG.
    J Am Chem Soc; 2012 Apr 18; 134(15):6741-50. PubMed ID: 22452319
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  • 2. Explaining Anomalies in Enamine Catalysis: "Downstream Species" as a New Paradigm for Stereocontrol.
    Burés J, Armstrong A, Blackmond DG.
    Acc Chem Res; 2016 Feb 16; 49(2):214-22. PubMed ID: 26830669
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  • 5. Mechanistic investigation of the 2,5-diphenylpyrrolidine-catalyzed enantioselective alpha-chlorination of aldehydes.
    Halland N, Alstrup Lie M, Kjaersgaard A, Marigo M, Schiøtt B, Jørgensen KA.
    Chemistry; 2005 Nov 18; 11(23):7083-90. PubMed ID: 16220562
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  • 8. Monitoring Reaction Intermediates to Predict Enantioselectivity Using Mass Spectrometry.
    Hilgers R, Yong Teng S, Briš A, Pereverzev AY, White P, Jansen JJ, Roithová J.
    Angew Chem Int Ed Engl; 2022 Sep 05; 61(36):e202205720. PubMed ID: 35561144
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  • 9. Extending NHC-catalysis: coupling aldehydes with unconventional reaction partners.
    Biju AT, Kuhl N, Glorius F.
    Acc Chem Res; 2011 Nov 15; 44(11):1182-95. PubMed ID: 21751790
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  • 15. Alpha,alpha-diarylprolinol ethers: new tools for functionalization of carbonyl compounds.
    Mielgo A, Palomo C.
    Chem Asian J; 2008 Jun 02; 3(6):922-48. PubMed ID: 18504714
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  • 16. Efficient, enantioselective iminium catalysis with an immobilized, recyclable diarylprolinol silyl ether catalyst.
    Mager I, Zeitler K.
    Org Lett; 2010 Apr 02; 12(7):1480-3. PubMed ID: 20201561
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  • 18. Adapting to substrate challenges: peptides as catalysts for conjugate addition reactions of aldehydes to α,β-disubstituted nitroolefins.
    Duschmalé J, Wennemers H.
    Chemistry; 2012 Jan 23; 18(4):1111-20. PubMed ID: 22189758
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  • 19. Peptide-catalyzed 1,4-addition reactions of aldehydes to nitroolefins.
    Kastl R, Arakawa Y, Duschmalé J, Wiesner M, Wennemers H.
    Chimia (Aarau); 2013 Jan 23; 67(4):279-82. PubMed ID: 23967706
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