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Journal Abstract Search

214 related items for PubMed ID: 23962962

  • 1. CuBr for KA(2) reaction: en route to propargylic amines bearing a quaternary carbon center.
    Tang X, Kuang J, Ma S.
    Chem Commun (Camb); 2013 Oct 11; 49(79):8976-8. PubMed ID: 23962962
    [Abstract] [Full Text] [Related]

  • 2. Copper/titanium catalysis forms fully substituted carbon centers from the direct coupling of acyclic ketones, amines, and alkynes.
    Pierce CJ, Nguyen M, Larsen CH.
    Angew Chem Int Ed Engl; 2012 Dec 03; 51(49):12289-92. PubMed ID: 23109121
    [No Abstract] [Full Text] [Related]

  • 3. Unprecedented Cu(I)-catalyzed microwave-assisted three-component coupling of a ketone, an alkyne, and a primary amine.
    Pereshivko OP, Peshkov VA, Van der Eycken EV.
    Org Lett; 2010 Jun 04; 12(11):2638-41. PubMed ID: 20441203
    [Abstract] [Full Text] [Related]

  • 4. An easily removable stereo-dictating group for enantioselective synthesis of propargylic amines.
    Fan W, Ma S.
    Chem Commun (Camb); 2013 Oct 03; 49(86):10175-7. PubMed ID: 24051867
    [Abstract] [Full Text] [Related]

  • 5. Copper-catalyzed enantioselective three-component synthesis of optically active propargylamines from aldehydes, amines, and aliphatic alkynes.
    Nakamura S, Ohara M, Nakamura Y, Shibata N, Toru T.
    Chemistry; 2010 Feb 22; 16(8):2360-2. PubMed ID: 20108286
    [No Abstract] [Full Text] [Related]

  • 6. Practical highly enantioselective synthesis of propargylamines through a copper-catalyzed one-pot three-component condensation reaction.
    Gommermann N, Knochel P.
    Chemistry; 2006 May 24; 12(16):4380-92. PubMed ID: 16557623
    [Abstract] [Full Text] [Related]

  • 7. Chemoselective C-H bond activation: ligand and solvent free iron-catalyzed oxidative C-C cross-coupling of tertiary amines with terminal alkynes. Reaction scope and mechanism.
    Volla CM, Vogel P.
    Org Lett; 2009 Apr 16; 11(8):1701-4. PubMed ID: 19296636
    [Abstract] [Full Text] [Related]

  • 8. An efficient synthesis of propargylamines via C-H activation catalyzed by copper(I) in ionic liquids.
    Park SB, Alper H.
    Chem Commun (Camb); 2005 Mar 14; (10):1315-7. PubMed ID: 15742063
    [Abstract] [Full Text] [Related]

  • 9. A simple method for the preparation of propargylamines using molecular sieve modified with copper(II).
    Fodor A, Kiss A, Debreczeni N, Hell Z, Gresits I.
    Org Biomol Chem; 2010 Oct 21; 8(20):4575-81. PubMed ID: 20740243
    [Abstract] [Full Text] [Related]

  • 10. Efficient iron(III)-catalyzed three-component coupling reaction of alkynes, CH2Cl2 and amines to propargylamines.
    Gao J, Song QW, He LN, Yang ZZ, Dou XY.
    Chem Commun (Camb); 2012 Feb 14; 48(14):2024-6. PubMed ID: 22234426
    [Abstract] [Full Text] [Related]

  • 11. The Asymmetric A³(Aldehyde⁻Alkyne⁻Amine) Coupling: Highly Enantioselective Access to Propargylamines.
    Mo JN, Su J, Zhao J.
    Molecules; 2019 Mar 28; 24(7):. PubMed ID: 30925732
    [Abstract] [Full Text] [Related]

  • 12. Efficient synthesis of propargylamines from terminal alkynes, dichloromethane and tertiary amines over silver catalysts.
    Chen X, Chen T, Zhou Y, Au CT, Han LB, Yin SF.
    Org Biomol Chem; 2014 Jan 14; 12(2):247-50. PubMed ID: 24264798
    [Abstract] [Full Text] [Related]

  • 13. Iron(III)-catalyzed and air-mediated tandem reaction of aldehydes, alkynes and amines: an efficient approach to substituted quinolines.
    Cao K, Zhang FM, Tu YQ, Zhuo XT, Fan CA.
    Chemistry; 2009 Jun 22; 15(26):6332-4. PubMed ID: 19472236
    [Abstract] [Full Text] [Related]

  • 14. Synthesis of tertiary propargylamines via a rationally designed multicomponent reaction of primary amines, formaldehyde, arylboronic acids and alkynes.
    Wang J, Shen Q, Li P, Peng Y, Song G.
    Org Biomol Chem; 2014 Aug 14; 12(30):5597-600. PubMed ID: 24969221
    [Abstract] [Full Text] [Related]

  • 15. Synthesis of enantiomerically enriched propargylamines by copper-catalyzed addition of alkynes to enamines.
    Koradin C, Gommermann N, Polborn K, Knochel P.
    Chemistry; 2003 Jun 16; 9(12):2797-2811. PubMed ID: 12866545
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