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Journal Abstract Search

302 related items for PubMed ID: 18444616

  • 1. Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate.
    Kim IS, Ngai MY, Krische MJ.
    J Am Chem Soc; 2008 May 21; 130(20):6340-1. PubMed ID: 18444616
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  • 3. 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 25; 131(7):2514-20. PubMed ID: 19191498
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  • 4. anti-Diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol or aldehyde oxidation level: allyl carbonates as allylmetal surrogates.
    Zhang YJ, Yang JH, Kim SH, Krische MJ.
    J Am Chem Soc; 2010 Apr 07; 132(13):4562-3. PubMed ID: 20225853
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  • 5. 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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  • 6. Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol or aldehyde oxidation level.
    Han SB, Gao X, Krische MJ.
    J Am Chem Soc; 2010 Jul 07; 132(26):9153-6. PubMed ID: 20540509
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  • 7. 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 21; (47):7278-87. PubMed ID: 20024203
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  • 8. 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 27; 131(20):6916-7. PubMed ID: 19453190
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  • 10. Enhanced anti-diastereo- and enantioselectivity in alcohol-mediated carbonyl crotylation using an isolable single component iridium catalyst.
    Gao X, Townsend IA, Krische MJ.
    J Org Chem; 2011 Apr 01; 76(7):2350-4. PubMed ID: 21375283
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  • 11. Diastereo- and Enantioselective Iridium Catalyzed Coupling of Vinyl Aziridines with Alcohols: Site-Selective Modification of Unprotected Diols and Synthesis of Substituted Piperidines.
    Wang G, Franke J, Ngo CQ, Krische MJ.
    J Am Chem Soc; 2015 Jun 24; 137(24):7915-20. PubMed ID: 26074091
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  • 15. Iridium-catalyzed allylation of chiral β-stereogenic alcohols: bypassing discrete formation of epimerizable aldehydes.
    Schmitt DC, Dechert-Schmitt AM, Krische MJ.
    Org Lett; 2012 Dec 21; 14(24):6302-5. PubMed ID: 23231774
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  • 16. Enantioselective conversion of primary alcohols to α-exo-methylene γ-butyrolactones via iridium-catalyzed C-C bond-forming transfer hydrogenation: 2-(alkoxycarbonyl)allylation.
    Montgomery TP, Hassan A, Park BY, Krische MJ.
    J Am Chem Soc; 2012 Jul 11; 134(27):11100-3. PubMed ID: 22734694
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  • 17. Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (α-trifluoromethyl)allylation from the alcohol or aldehyde oxidation level.
    Gao X, Zhang YJ, Krische MJ.
    Angew Chem Int Ed Engl; 2011 Apr 26; 50(18):4173-5. PubMed ID: 21472938
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  • 18. Selection between Diastereomeric Kinetic vs Thermodynamic Carbonyl Binding Modes Enables Enantioselective Iridium-Catalyzed anti-(α-Aryl)allylation of Aqueous Fluoral Hydrate and Difluoroacetaldehyde Ethyl Hemiacetal.
    Cabrera JM, Tauber J, Zhang W, Xiang M, Krische MJ.
    J Am Chem Soc; 2018 Aug 01; 140(30):9392-9395. PubMed ID: 30020777
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