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Journal Abstract Search

1061 related items for PubMed ID: 28809470

  • 1. Chelation-Controlled Additions to Chiral α- and β-Silyloxy, α-Halo, and β-Vinyl Carbonyl Compounds.
    Fan X, Walsh PJ.
    Acc Chem Res; 2017 Sep 19; 50(9):2389-2400. PubMed ID: 28809470
    [Abstract] [Full Text] [Related]

  • 2. Highly diastereoselective chelation-controlled additions to α-silyloxy ketones.
    Stanton GR, Koz G, Walsh PJ.
    J Am Chem Soc; 2011 May 25; 133(20):7969-76. PubMed ID: 21534530
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  • 3. Overriding Felkin control: a general method for highly diastereoselective chelation-controlled additions to alpha-silyloxy aldehydes.
    Stanton GR, Johnson CN, Walsh PJ.
    J Am Chem Soc; 2010 Mar 31; 132(12):4399-408. PubMed ID: 20218659
    [Abstract] [Full Text] [Related]

  • 4. Chelation-controlled additions to α-silyloxy aldehydes: an autocatalytic approach.
    Raffier L, Stanton GR, Walsh PJ.
    Org Lett; 2013 Dec 20; 15(24):6174-7. PubMed ID: 24252100
    [Abstract] [Full Text] [Related]

  • 5. Chelation-controlled addition of organozincs to α-chloro aldimines.
    Stanton GR, Norrby PO, Carroll PJ, Walsh PJ.
    J Am Chem Soc; 2012 Oct 24; 134(42):17599-604. PubMed ID: 23003333
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  • 6. Catalytic asymmetric organozinc additions to carbonyl compounds.
    Pu L, Yu HB.
    Chem Rev; 2001 Mar 24; 101(3):757-824. PubMed ID: 11712502
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  • 8. The exceptional chelating ability of dimethylaluminum chloride and methylaluminum dichloride. The merged stereochemical impact of alpha- and beta-stereocenters in chelate-controlled carbonyl addition reactions with enolsilane and hydride nucleophiles.
    Evans DA, Allison BD, Yang MG, Masse CE.
    J Am Chem Soc; 2001 Nov 07; 123(44):10840-52. PubMed ID: 11686685
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  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. Diastereoselective additions of chiral vinylzinc reagents to alpha-chiral aldehydes.
    Marshall JA, Eidam P.
    Org Lett; 2004 Feb 05; 6(3):445-8. PubMed ID: 14748614
    [Abstract] [Full Text] [Related]

  • 12. Asymmetric induction in methyl ketone aldol additions to alpha-alkoxy and alpha,beta-bisalkoxy aldehydes: a model for acyclic stereocontrol.
    Evans DA, Cee VJ, Siska SJ.
    J Am Chem Soc; 2006 Jul 26; 128(29):9433-41. PubMed ID: 16848480
    [Abstract] [Full Text] [Related]

  • 13. Asymmetric functional organozinc additions to aldehydes catalyzed by 1,1'-bi-2-naphthols (BINOLs).
    Pu L.
    Acc Chem Res; 2014 May 20; 47(5):1523-35. PubMed ID: 24738985
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  • 18. Asymmetric Cycloaddition and Cyclization Reactions Catalyzed by Chiral N,N'-Dioxide-Metal Complexes.
    Liu X, Zheng H, Xia Y, Lin L, Feng X.
    Acc Chem Res; 2017 Oct 17; 50(10):2621-2631. PubMed ID: 28967737
    [Abstract] [Full Text] [Related]

  • 19. Catalytic Enantioselective Hydrovinylation of Trialkylsilyloxy and Acetoxy-1,3-Dienes: Cationic Co(I) Complexes for the Synthesis of Chiral Enolate Surrogates and Their Applications for Synthesis of Ketones and Cross-Coupling Reagents in High Enantiomeric Purity.
    Biswas S, Dewese KR, Raya B, RajanBabu TV.
    ACS Catal; 2022 May 06; 12(9):5094-5111. PubMed ID: 36110156
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  • 20. Chiral N,N'-dioxides: new ligands and organocatalysts for catalytic asymmetric reactions.
    Liu X, Lin L, Feng X.
    Acc Chem Res; 2011 Aug 16; 44(8):574-87. PubMed ID: 21702458
    [Abstract] [Full Text] [Related]

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