BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

345 related articles for article (PubMed ID: 27113543)

  • 1. Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis.
    Feng J; Kasun ZA; Krische MJ
    J Am Chem Soc; 2016 May; 138(17):5467-78. PubMed ID: 27113543
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Catalytic Enantioselective Carbonyl Allylation and Propargylation via Alcohol-Mediated Hydrogen Transfer: Merging the Chemistry of Grignard and Sabatier.
    Kim SW; Zhang W; Krische MJ
    Acc Chem Res; 2017 Sep; 50(9):2371-2380. PubMed ID: 28792731
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: borrowing hydrogen, returning carbon.
    Ketcham JM; Shin I; Montgomery TP; Krische MJ
    Angew Chem Int Ed Engl; 2014 Aug; 53(35):9142-50. PubMed ID: 25056771
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Asymmetric Iridium-Catalyzed C-C Coupling of Chiral Diols via Site-Selective Redox-Triggered Carbonyl Addition.
    Shin I; Krische MJ
    Top Curr Chem; 2016; 372():85-101. PubMed ID: 26187028
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Total Synthesis of Clavosolide A via Asymmetric Alcohol-Mediated Carbonyl Allylation: Beyond Protecting Groups or Chiral Auxiliaries in Polyketide Construction.
    Cabrera JM; Krische MJ
    Angew Chem Int Ed Engl; 2019 Jul; 58(31):10718-10722. PubMed ID: 31166641
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Unlocking Hydrogenation for C-C Bond Formation: A Brief Overview of Enantioselective Methods.
    Hassan A; Krische MJ
    Org Process Res Dev; 2011 Nov; 15(6):1236-1242. PubMed ID: 22125398
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Formation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation.
    Bower JF; Krische MJ
    Top Organomet Chem; 2011 Jan; 34(2011):107-138. PubMed ID: 21822399
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiency.
    Han SB; Kim IS; Krische MJ
    Chem Commun (Camb); 2009 Dec; (47):7278-87. PubMed ID: 20024203
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Polyketide construction via hydrohydroxyalkylation and related alcohol C-H functionalizations: reinventing the chemistry of carbonyl addition.
    Dechert-Schmitt AM; Schmitt DC; Gao X; Itoh T; Krische MJ
    Nat Prod Rep; 2014 Apr; 31(4):504-13. PubMed ID: 24514754
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ruthenium-Catalyzed Transfer Hydrogenation for C-C Bond Formation: Hydrohydroxyalkylation and Hydroaminoalkylation via Reactant Redox Pairs.
    Perez F; Oda S; Geary LM; Krische MJ
    Top Curr Chem (Cham); 2016 Jun; 374(3):35. PubMed ID: 27573275
    [TBL] [Abstract][Full Text] [Related]  

  • 11. anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents.
    Kim IS; Han SB; Krische MJ
    J Am Chem Soc; 2009 Feb; 131(7):2514-20. PubMed ID: 19191498
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Protecting-group-free diastereoselective C-C coupling of 1,3-glycols and allyl acetate through site-selective primary alcohol dehydrogenation.
    Dechert-Schmitt AM; Schmitt DC; Krische MJ
    Angew Chem Int Ed Engl; 2013 Mar; 52(11):3195-8. PubMed ID: 23364927
    [No Abstract]   [Full Text] [Related]  

  • 13. Total Synthesis of Leiodermatolide A via Transfer Hydrogenative Allylation, Crotylation, and Propargylation: Polyketide Construction beyond Discrete Allyl- or Allenylmetal Reagents.
    Siu YM; Roane J; Krische MJ
    J Am Chem Soc; 2021 Jul; 143(28):10590-10595. PubMed ID: 34237219
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor.
    Han SB; Kim IS; Han H; Krische MJ
    J Am Chem Soc; 2009 May; 131(20):6916-7. PubMed ID: 19453190
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Redox-triggered C-C coupling of alcohols and vinyl epoxides: diastereo- and enantioselective formation of all-carbon quaternary centers via tert-(hydroxy)-prenylation.
    Feng J; Garza VJ; Krische MJ
    J Am Chem Soc; 2014 Jun; 136(25):8911-4. PubMed ID: 24915473
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Formation of C-C bonds via ruthenium-catalyzed transfer hydrogenation().
    Moran J; Krische MJ
    Pure Appl Chem; 2012; 84(8):1729-1739. PubMed ID: 23430602
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Enantioselective ruthenium-catalyzed carbonyl allylation via alkyne-alcohol C-C bond-forming transfer hydrogenation: allene hydrometalation vs oxidative coupling.
    Liang T; Nguyen KD; Zhang W; Krische MJ
    J Am Chem Soc; 2015 Mar; 137(9):3161-4. PubMed ID: 25734220
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Direct generation of acyclic polypropionate stereopolyads via double diastereo- and enantioselective iridium-catalyzed crotylation of 1,3-diols: beyond stepwise carbonyl addition in polyketide construction.
    Gao X; Han H; Krische MJ
    J Am Chem Soc; 2011 Aug; 133(32):12795-800. PubMed ID: 21739988
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Formation of C-C Bonds via Ruthenium Catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation Level.
    Shibahara F; Krische MJ
    Chem Lett; 2008; 37(11):1102-1107. PubMed ID: 21927534
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Enantioselective carbonyl propargylation by iridium-catalyzed transfer hydrogenative coupling of alcohols and propargyl chlorides.
    Woo SK; Geary LM; Krische MJ
    Angew Chem Int Ed Engl; 2012 Jul; 51(31):7830-4. PubMed ID: 22736416
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.