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Journal Abstract Search

471 related items for PubMed ID: 10655780

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  • 2. [Development of highly stereoselective reactions utilizing heteroatoms--new approach to the stereoselective Horner-Wadsworth-Emmons reaction].
    Sano S.
    Yakugaku Zasshi; 2000 May; 120(5):432-44. PubMed ID: 10825807
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  • 3. Oxazinanones as chiral auxiliaries: synthesis and evaluation in enolate alkylations and aldol reactions.
    Davies SG, Garner AC, Roberts PM, Smith AD, Sweet MJ, Thomson JE.
    Org Biomol Chem; 2006 Jul 21; 4(14):2753-68. PubMed ID: 16826300
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  • 4. Microbial/enzymatic synthesis of chiral drug intermediates.
    Patel RN.
    Adv Appl Microbiol; 2000 Jul 21; 47():33-78. PubMed ID: 12876794
    [Abstract] [Full Text] [Related]

  • 5. Asymmetric total synthesis of (-)-callystatin A and (-)-20-epi-callystatin A employing chemical and biological methods.
    Enders D, Vicario JL, Job A, Wolberg M, Müller M.
    Chemistry; 2002 Sep 16; 8(18):4272-84. PubMed ID: 12298019
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  • 7. Steering Asymmetric Lewis Acid Catalysis Exclusively with Octahedral Metal-Centered Chirality.
    Zhang L, Meggers E.
    Acc Chem Res; 2017 Feb 21; 50(2):320-330. PubMed ID: 28128920
    [Abstract] [Full Text] [Related]

  • 8. [Development of asymmetric synthesis of optically active compounds including fluoroorganic molecules].
    Iseki K.
    Yakugaku Zasshi; 1999 Nov 21; 119(11):787-804. PubMed ID: 10590709
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  • 10. Catalytic enantioselective alkylative aldol reaction: efficient multicomponent assembly of dialkylzincs, allenic esters, and ketones toward highly functionalized delta-lactones with tetrasubstituted chiral centers.
    Oisaki K, Zhao D, Kanai M, Shibasaki M.
    J Am Chem Soc; 2007 Jun 13; 129(23):7439-43. PubMed ID: 17503823
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  • 11. Direct catalytic enantio- and diastereoselective aldol reaction of thioamides.
    Iwata M, Yazaki R, Chen IH, Sureshkumar D, Kumagai N, Shibasaki M.
    J Am Chem Soc; 2011 Apr 13; 133(14):5554-60. PubMed ID: 21417332
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  • 15. Organocatalytic asymmetric aldol reaction of hydroxyacetone with β,γ-unsaturated α-keto esters: facile access to chiral tertiary alcohols.
    Liu C, Dou X, Lu Y.
    Org Lett; 2011 Oct 07; 13(19):5248-51. PubMed ID: 21902199
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