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Journal Abstract Search

361 related items for PubMed ID: 22497595

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  • 2. Indium-mediated asymmetric barbier-type allylations: additions to aldehydes and ketones and mechanistic investigation of the organoindium reagents.
    Haddad TD, Hirayama LC, Singaram B.
    J Org Chem; 2010 Feb 05; 75(3):642-9. PubMed ID: 20027999
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  • 3. Indium-mediated asymmetric Barbier-type propargylations: additions to aldehydes and ketones and mechanistic investigation of the organoindium reagents.
    Haddad TD, Hirayama LC, Buckley JJ, Singaram B.
    J Org Chem; 2012 Jan 20; 77(2):889-98. PubMed ID: 22148263
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  • 5. An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines.
    Lin GQ, Xu MH, Zhong YW, Sun XW.
    Acc Chem Res; 2008 Jul 20; 41(7):831-40. PubMed ID: 18533688
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  • 9. Control of skeletal connectivity in indium promoted reactions: 1,2-additions and cope rearrangements en route to lactol formation.
    Mitzel T, Wzorek J, Troutman A, Allegue K.
    J Org Chem; 2007 Apr 13; 72(8):3042-52. PubMed ID: 17348712
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  • 14. "Design" of boron-based compounds as pro-nucleophiles and co-catalysts for indium(I)-catalyzed allyl transfer to various Csp3-type electrophiles.
    Dao HT, Schneider U, Kobayashi S.
    Chem Asian J; 2011 Sep 05; 6(9):2522-9. PubMed ID: 21728247
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  • 15. Magnesium-Mediated Carbon-Carbon Bond Formation in Aqueous Media: Barbier-Grignard Allylation and Pinacol Coupling of Aldehydes.
    Zhang WC, Li CJ.
    J Org Chem; 1999 Apr 30; 64(9):3230-3236. PubMed ID: 11674425
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  • 16. Indium-mediated beta-allylation, beta-propargylation, and beta-allenylation onto alpha,beta-unsaturated ketones: reactions of in-situ-generated 3-tert-butyldimethylsilyloxyalk-2-enylsulfonium salts with in-situ-generated organoindium reagents.
    Lee K, Kim H, Miura T, Kiyota K, Kusama H, Kim S, Iwasawa N, Lee PH.
    J Am Chem Soc; 2003 Aug 13; 125(32):9682-8. PubMed ID: 12904034
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  • 17. Rhodium-catalyzed allylation of aldehydes with homoallylic alcohols by retroallylation and isomerization to saturated ketones with conventional or microwave heating.
    Sumida Y, Takada Y, Hayashi S, Hirano K, Yorimitsu H, Oshima K.
    Chem Asian J; 2008 Jan 04; 3(1):119-25. PubMed ID: 18034441
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  • 20. Hydride as a leaving group in the reaction of pinacolborane with halides under ambient Grignard and Barbier conditions. One-pot synthesis of alkyl, aryl, heteroaryl, vinyl, and allyl pinacolboronic esters.
    Clary JW, Rettenmaier TJ, Snelling R, Bryks W, Banwell J, Wipke WT, Singaram B.
    J Org Chem; 2011 Dec 02; 76(23):9602-10. PubMed ID: 22040316
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