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556 related items for PubMed ID: 23379769

  • 1. Atom-economical chemoselective synthesis of 1,4-enynes from terminal alkenes and propargylic alcohols catalyzed by Cu(OTf)2.
    Huang GB, Wang X, Pan YM, Wang HS, Yao GY, Zhang Y.
    J Org Chem; 2013 Mar 15; 78(6):2742-5. PubMed ID: 23379769
    [Abstract] [Full Text] [Related]

  • 2. Nickel-catalyzed enantioselective alkylative coupling of alkynes and aldehydes: synthesis of chiral allylic alcohols with tetrasubstituted olefins.
    Yang Y, Zhu SF, Zhou CY, Zhou QL.
    J Am Chem Soc; 2008 Oct 29; 130(43):14052-3. PubMed ID: 18834121
    [Abstract] [Full Text] [Related]

  • 3. Novel carbon-carbon bond formation from propargylic alcohols and olefin toward five-membered heterocyclic rings catalyzed by AgSbF6.
    Ji KG, Shu XZ, Zhao SC, Zhu HT, Niu YN, Liu XY, Liang YM.
    Org Lett; 2009 Aug 06; 11(15):3206-9. PubMed ID: 19572605
    [Abstract] [Full Text] [Related]

  • 4. Controllable stereoselective synthesis of trisubstituted alkenes by a catalytic three-component reaction of terminal alkynes, benzylic alcohols, and simple arenes.
    Li HH, Jin YH, Wang JQ, Tian SK.
    Org Biomol Chem; 2009 Aug 21; 7(16):3219-21. PubMed ID: 19641777
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  • 5. Highly chemoselective calcium-catalyzed propargylic deoxygenation.
    Meyer VJ, Niggemann M.
    Chemistry; 2012 Apr 10; 18(15):4687-91. PubMed ID: 22378484
    [Abstract] [Full Text] [Related]

  • 6. Propargyl alcohols as β-oxocarbenoid precursors for the ruthenium-catalyzed cyclopropanation of unactivated olefins by redox isomerization.
    Trost BM, Breder A, O'Keefe BM, Rao M, Franz AW.
    J Am Chem Soc; 2011 Apr 06; 133(13):4766-9. PubMed ID: 21401098
    [Abstract] [Full Text] [Related]

  • 7. Chemoselective synthesis of substituted pyrazoles through AgOTf-catalyzed cascade propargylic substitution-cyclization-aromatization.
    Xu SX, Hao L, Wang T, Ding ZC, Zhan ZP.
    Org Biomol Chem; 2013 Jan 14; 11(2):294-8. PubMed ID: 23188378
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  • 9. Ytterbium(III) triflate catalyzed tandem Friedel-Crafts alkylation/hydroarylation of propargylic alcohols with phenols as an expedient route to indenols.
    Zhang X, Teo WT, Chan PW.
    Org Lett; 2009 Nov 05; 11(21):4990-3. PubMed ID: 19863152
    [Abstract] [Full Text] [Related]

  • 10. An atom-economical access to β-heteroarylated ketones from propargylic alcohols via tandem ruthenium/indium catalysis.
    Trost BM, Breder A.
    Org Lett; 2011 Feb 04; 13(3):398-401. PubMed ID: 21190354
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  • 12. Lewis acid-catalyzed cyclization of enaminones with propargylic alcohols: regioselective synthesis of multisubstituted 1,2-dihydropyridines.
    Shao Y, Zhu K, Qin Z, Li E, Li Y.
    J Org Chem; 2013 Jun 07; 78(11):5731-6. PubMed ID: 23651059
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  • 15. Brønsted acid catalyzed cyclization of propargylic alcohols with thioamides. Facile synthesis of di- and trisubstituted thiazoles.
    Zhang X, Teo WT, Sally, Chan PW.
    J Org Chem; 2010 Sep 17; 75(18):6290-3. PubMed ID: 20795628
    [Abstract] [Full Text] [Related]

  • 16. Rhodium-catalyzed asymmetric tandem cyclization for efficient and rapid access to underexplored heterocyclic tertiary allylic alcohols containing a tetrasubstituted olefin.
    Li Y, Xu MH.
    Org Lett; 2014 May 16; 16(10):2712-5. PubMed ID: 24772999
    [Abstract] [Full Text] [Related]

  • 17. Highly efficient synthesis of tri- and tetrasubstituted conjugated enynes from Brønsted acid catalyzed alkoxylation of 1-cyclopropylprop-2-yn-1-ols with alcohols.
    Mothe SR, Chan PW.
    J Org Chem; 2009 Aug 21; 74(16):5887-93. PubMed ID: 19630423
    [Abstract] [Full Text] [Related]

  • 18. Remarkable access to fluoroalkylated trisubstituted alkenes via highly stereoselective cobalt-catalyzed hydrosilylation reaction of fluoroalkylated alkynes.
    Konno T, Taku K, Yamada S, Moriyasu K, Ishihara T.
    Org Biomol Chem; 2009 Mar 21; 7(6):1167-70. PubMed ID: 19262936
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  • 20. Highly stereoselective palladium-catalyzed dithiocarbonylation of propargylic mesylates with thiols and carbon monoxide.
    Xiao WJ, Alper H.
    J Org Chem; 2005 Mar 04; 70(5):1802-7. PubMed ID: 15730305
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