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719 related items for PubMed ID: 17402733

  • 1. Kinetic and computational analysis of the palladium(II)-catalyzed asymmetric allylic trichloroacetimidate rearrangement: development of a model for enantioselectivity.
    Watson MP, Overman LE, Bergman RG.
    J Am Chem Soc; 2007 Apr 25; 129(16):5031-44. PubMed ID: 17402733
    [Abstract] [Full Text] [Related]

  • 2. Catalytic asymmetric rearrangement of allylic trichloroacetimidates. A practical method for preparing allylic amines and congeners of high enantiomeric purity.
    Anderson CE, Overman LE.
    J Am Chem Soc; 2003 Oct 15; 125(41):12412-3. PubMed ID: 14531676
    [Abstract] [Full Text] [Related]

  • 3. Palladium(II)-Catalyzed Enantioselective Reactions Using COP Catalysts.
    Cannon JS, Overman LE.
    Acc Chem Res; 2016 Oct 18; 49(10):2220-2231. PubMed ID: 27689745
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  • 4. Palladacyclic imidazoline-naphthalene complexes: synthesis and catalytic performance in Pd(II)-catalyzed enantioselective reactions of allylic trichloroacetimidates.
    Cannon JS, Frederich JH, Overman LE.
    J Org Chem; 2012 Feb 17; 77(4):1939-51. PubMed ID: 22288535
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  • 5. Highly selective palladium catalyzed kinetic resolution and enantioselective substitution of racemic allylic carbonates with sulfur nucleophiles: asymmetric synthesis of allylic sulfides, allylic sulfones, and allylic alcohols.
    Gais HJ, Jagusch T, Spalthoff N, Gerhards F, Frank M, Raabe G.
    Chemistry; 2003 Sep 05; 9(17):4202-21. PubMed ID: 12953206
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  • 6. Palladium-catalyzed allylic transposition of (allyloxy) iminodiazaphospholidines: a formal [3,3]-aza-phospha-oxa-Cope sigmatropic rearrangement for the stereoselective synthesis of allylic amines.
    Lee EE, Batey RA.
    J Am Chem Soc; 2005 Oct 26; 127(42):14887-93. PubMed ID: 16231944
    [Abstract] [Full Text] [Related]

  • 7. The asymmetric aza-Claisen rearrangement: development of widely applicable pentaphenylferrocenyl palladacycle catalysts.
    Fischer DF, Barakat A, Xin ZQ, Weiss ME, Peters R.
    Chemistry; 2009 Sep 07; 15(35):8722-41. PubMed ID: 19691065
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  • 8. Catalytic asymmetric rearrangement of allylic N-aryl trifluoroacetimidates. A useful method for transforming prochiral allylic alcohols to chiral allylic amines.
    Overman LE, Owen CE, Pavan MM, Richards CJ.
    Org Lett; 2003 May 29; 5(11):1809-12. PubMed ID: 12762658
    [Abstract] [Full Text] [Related]

  • 9. Development of aliphatic alcohols as nucleophiles for palladium-catalyzed DYKAT reactions: total synthesis of (+)-hippospongic acid A.
    Trost BM, Machacek MR, Tsui HC.
    J Am Chem Soc; 2005 May 18; 127(19):7014-24. PubMed ID: 15884945
    [Abstract] [Full Text] [Related]

  • 10. Palladium(II)-catalyzed rearrangement of glycal trichloroacetimidates: application to the stereoselective synthesis of glycosyl ureas.
    Mercer GJ, Yang J, McKay MJ, Nguyen HM.
    J Am Chem Soc; 2008 Aug 20; 130(33):11210-8. PubMed ID: 18642810
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  • 12. Synthesis of nearly enantiopure allylic amines by aza-Claisen rearrangement of Z-configured allylic trifluoroacetimidates catalyzed by highly active ferrocenylbispalladacycles.
    Jautze S, Seiler P, Peters R.
    Chemistry; 2008 Aug 20; 14(5):1430-44. PubMed ID: 18098234
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  • 13. Catalytic asymmetric synthesis of chiral allylic amines. Evaluation of ferrocenyloxazoline palladacycle catalysts and imidate motifs.
    Anderson CE, Donde Y, Douglas CJ, Overman LE.
    J Org Chem; 2005 Jan 21; 70(2):648-57. PubMed ID: 15651813
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  • 15. Novel C2-symmetric planar chiral diphosphine ligands and their application in pd-catalyzed asymmetric allylic substitutions.
    Liu D, Xie F, Zhang W.
    J Org Chem; 2007 Aug 31; 72(18):6992-7. PubMed ID: 17676916
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  • 19. Dual Palladium(II)/Tertiary Amine Catalysis for Asymmetric Regioselective Rearrangements of Allylic Carbamates.
    Bauer JM, Frey W, Peters R.
    Chemistry; 2016 Apr 11; 22(16):5767-77. PubMed ID: 26990446
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  • 20. Structure-based rationale for selectivity in the asymmetric allylic alkylation of cycloalkenyl esters employing the Trost 'Standard Ligand' (TSL): isolation, analysis and alkylation of the monomeric form of the cationic eta(3)-cyclohexenyl complex [(eta(3)-c-C6H9)Pd(TSL)]+.
    Butts CP, Filali E, Lloyd-Jones GC, Norrby PO, Sale DA, Schramm Y.
    J Am Chem Soc; 2009 Jul 29; 131(29):9945-57. PubMed ID: 19435358
    [Abstract] [Full Text] [Related]

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