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Journal Abstract Search

304 related items for PubMed ID: 18841895

  • 1. Diene hydroacylation from the alcohol or aldehyde oxidation level via ruthenium-catalyzed C-C bond-forming transfer hydrogenation: synthesis of beta,gamma-unsaturated ketones.
    Shibahara F, Bower JF, Krische MJ.
    J Am Chem Soc; 2008 Oct 29; 130(43):14120-2. PubMed ID: 18841895
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  • 2. Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents.
    Shibahara F, Bower JF, Krische MJ.
    J Am Chem Soc; 2008 May 21; 130(20):6338-9. PubMed ID: 18444617
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  • 3. Hydroacylation of 2-Butyne from the Alcohol or Aldehyde Oxidation Level via Ruthenium Catalyzed C-C Bond Forming Transfer Hydrogenation.
    Williams VM, Leung JC, Patman RL, Krische MJ.
    Tetrahedron; 2009 Jun 27; 65(26):5024-5029. PubMed ID: 20613891
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  • 4. Ruthenium catalyzed C-C bond formation via transfer hydrogenation: branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes.
    Ngai MY, Skucas E, Krische MJ.
    Org Lett; 2008 Jul 03; 10(13):2705-8. PubMed ID: 18533665
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  • 5. Ruthenium hydride-catalyzed addition of aldehydes to dienes leading to beta,gamma-unsaturated ketones.
    Omura S, Fukuyama T, Horiguchi J, Murakami Y, Ryu I.
    J Am Chem Soc; 2008 Oct 29; 130(43):14094-5. PubMed ID: 18841894
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  • 6. Direct vinylation of alcohols or aldehydes employing alkynes as vinyl donors: a ruthenium catalyzed C-C bond-forming transfer hydrogenation.
    Patman RL, Chaulagain MR, Williams VM, Krische MJ.
    J Am Chem Soc; 2009 Feb 18; 131(6):2066-7. PubMed ID: 19173651
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  • 7. Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene.
    Bower JF, Patman RL, Krische MJ.
    Org Lett; 2008 Mar 06; 10(5):1033-5. PubMed ID: 18254642
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  • 8. Successive C-C coupling of dienes to vicinally dioxygenated hydrocarbons: ruthenium catalyzed [4 + 2] cycloaddition across the diol, hydroxycarbonyl, or dione oxidation levels.
    Geary LM, Glasspoole BW, Kim MM, Krische MJ.
    J Am Chem Soc; 2013 Mar 13; 135(10):3796-9. PubMed ID: 23448269
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  • 10. anti-Aminoallylation of aldehydes via ruthenium-catalyzed transfer hydrogenative coupling of sulfonamido allenes: 1,2-aminoalcohols.
    Skucas E, Zbieg JR, Krische MJ.
    J Am Chem Soc; 2009 Apr 15; 131(14):5054-5. PubMed ID: 19317402
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  • 14. Amplification of anti-diastereoselectivity via Curtin-Hammett effects in ruthenium-catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes: diastereoselective formation of all-carbon quaternary centers.
    Zbieg JR, McInturff EL, Leung JC, Krische MJ.
    J Am Chem Soc; 2011 Feb 02; 133(4):1141-4. PubMed ID: 21175178
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  • 15. Regioselective Hydrohydroxyalkylation of Styrene with Primary Alcohols or Aldehydes via Ruthenium-Catalyzed C-C Bond Forming Transfer Hydrogenation.
    Xiao H, Wang G, Krische MJ.
    Angew Chem Int Ed Engl; 2016 Dec 23; 55(52):16119-16122. PubMed ID: 27910228
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  • 18. Highly active, immobilized ruthenium catalysts for oxidation of alcohols to aldehydes and ketones. Preparation and use in both batch and flow systems.
    Kobayashi S, Miyamura H, Akiyama R, Ishida T.
    J Am Chem Soc; 2005 Jun 29; 127(25):9251-4. PubMed ID: 15969605
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  • 20. Direct ruthenium-catalyzed C-C coupling of ethanol: diene hydro-hydroxyethylation to form all-carbon quaternary centers.
    Han H, Krische MJ.
    Org Lett; 2010 Jun 18; 12(12):2844-6. PubMed ID: 20491487
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