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220 related items for PubMed ID: 15453733

  • 1. A general bifunctional catalyst for the anti-Markovnikov hydration of terminal alkynes to aldehydes gives enzyme-like rate and selectivity enhancements.
    Grotjahn DB, Lev DA.
    J Am Chem Soc; 2004 Oct 06; 126(39):12232-3. PubMed ID: 15453733
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  • 3. [Ind(2)TiMe(2)]: a general catalyst for the intermolecular hydroamination of alkynes.
    Heutling A, Pohlki F, Doye S.
    Chemistry; 2004 Jun 21; 10(12):3059-71. PubMed ID: 15214090
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  • 4. Isolable gold(I) complexes having one low-coordinating ligand as catalysts for the selective hydration of substituted alkynes at room temperature without acidic promoters.
    Leyva A, Corma A.
    J Org Chem; 2009 Mar 06; 74(5):2067-74. PubMed ID: 19170603
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  • 6. A general study of [(eta5-Cp')2Ti(eta2-Me3SiC2SiMe3)]-catalyzed hydroamination of terminal alkynes: regioselective formation of Markovnikov and anti-Markovnikov products and mechanistic explanation (Cp'=C5H5, C5H4Et, C5Me5).
    Tillack A, Jiao H, Garcia Castro I, Hartung CG, Beller M.
    Chemistry; 2004 May 17; 10(10):2409-20. PubMed ID: 15146514
    [Abstract] [Full Text] [Related]

  • 7. Redox-neutral synthesis of beta-amino aldehydes from imines by an alkynylation/hydration sequence.
    Labonne A, Zani L, Hintermann L, Bolm C.
    J Org Chem; 2007 Jul 20; 72(15):5704-8. PubMed ID: 17595140
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  • 8. Highly active in situ catalysts for anti-Markovnikov hydration of terminal alkynes.
    Labonne A, Kribber T, Hintermann L.
    Org Lett; 2006 Dec 07; 8(25):5853-6. PubMed ID: 17134289
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  • 9. Organozirconium complexes as catalysts for Markovnikov-selective intermolecular hydrothiolation of terminal alkynes: scope and mechanism.
    Weiss CJ, Marks TJ.
    J Am Chem Soc; 2010 Aug 04; 132(30):10533-46. PubMed ID: 20617838
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  • 11. [(NHC)Au(I)]-catalyzed acid-free alkyne hydration at part-per-million catalyst loadings.
    Marion N, Ramón RS, Nolan SP.
    J Am Chem Soc; 2009 Jan 21; 131(2):448-9. PubMed ID: 19140786
    [Abstract] [Full Text] [Related]

  • 12. A highly active and air-stable ruthenium complex for the ambient temperature anti-Markovnikov reductive hydration of terminal alkynes.
    Zeng M, Li L, Herzon SB.
    J Am Chem Soc; 2014 May 14; 136(19):7058-67. PubMed ID: 24786693
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  • 14. TiCl4-catalyzed indirect anti-Markovnikov hydration of alkynes: application to the synthesis of benzo[b]furans.
    Ackermann L, Kaspar LT.
    J Org Chem; 2007 Aug 03; 72(16):6149-53. PubMed ID: 17629343
    [Abstract] [Full Text] [Related]

  • 15. Broad-spectrum catalysts for the ambient temperature anti-Markovnikov hydration of alkynes.
    Li L, Zeng M, Herzon SB.
    Angew Chem Int Ed Engl; 2014 Jul 21; 53(30):7892-5. PubMed ID: 24964738
    [Abstract] [Full Text] [Related]

  • 16. Re(CO)5Br-catalyzed addition of carboxylic acids to terminal alkynes: a high anti-Markovnikov and recoverable homogeneous catalyst.
    Hua R, Tian X.
    J Org Chem; 2004 Aug 20; 69(17):5782-4. PubMed ID: 15307759
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  • 18. Rhodium-catalyzed selective anti-Markovnikov addition of carboxylic acids to alkynes.
    Lumbroso A, Vautravers NR, Breit B.
    Org Lett; 2010 Dec 03; 12(23):5498-501. PubMed ID: 21049947
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  • 19. Combined Effects of Metal and Ligand Capable of Accepting a Proton or Hydrogen Bond Catalyze Anti-Markovnikov Hydration of Terminal Alkynes.
    Grotjahn DB, Incarvito CD, Rheingold AL.
    Angew Chem Int Ed Engl; 2001 Oct 15; 40(20):3884-3887. PubMed ID: 29712127
    [Abstract] [Full Text] [Related]

  • 20. Ruthenium-catalyzed hydrative cyclization of 1,5-enynes.
    Chen Y, Ho DM, Lee C.
    J Am Chem Soc; 2005 Sep 07; 127(35):12184-5. PubMed ID: 16131171
    [Abstract] [Full Text] [Related]

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