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222 related items for PubMed ID: 24919989
1. Direct enantioselective three-component synthesis of optically active propargylamines in water. Ohara M, Hara Y, Ohnuki T, Nakamura S. Chemistry; 2014 Jul 14; 20(29):8848-51. PubMed ID: 24919989 [Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Copper(I) halide promoted diastereoselective synthesis of chiral propargylamines and chiral allenes using 2-dialkylaminomethylpyrrolidine, aldehydes, and 1-alkynes. Gurubrahamam R, Periasamy M. J Org Chem; 2013 Feb 15; 78(4):1463-70. PubMed ID: 23320792 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
9. 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]
10. Highly enantioselective access to primary propargylamines: 4-piperidinone as a convenient protecting group. Aschwanden P, Stephenson CR, Carreira EM. Org Lett; 2006 May 25; 8(11):2437-40. PubMed ID: 16706545 [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]
16. Rapid one-pot propargylamine synthesis by plasmon mediated catalysis with gold nanoparticles on ZnO under ambient conditions. González-Béjar M, Peters K, Hallett-Tapley GL, Grenier M, Scaiano JC. Chem Commun (Camb); 2013 Feb 28; 49(17):1732-4. PubMed ID: 23340772 [Abstract] [Full Text] [Related]
17. Gold(III) Salen complex-catalyzed synthesis of propargylamines via a three-component coupling reaction. Lo VK, Liu Y, Wong MK, Che CM. Org Lett; 2006 Apr 13; 8(8):1529-32. PubMed ID: 16597102 [Abstract] [Full Text] [Related]
18. Enantioselective alkynylation of benzo[e][1,2,3]-oxathiazine 2,2-dioxides catalysed by (R)-VAPOL-Zn complexes: synthesis of chiral propargylic cyclic sulfamidates. De Munck L, Monleón A, Vila C, Muñoz MC, Pedro JR. Org Biomol Chem; 2015 Jul 21; 13(27):7393-6. PubMed ID: 26081255 [Abstract] [Full Text] [Related]
19. Enantioselective direct-addition of terminal alkynes to imines catalyzed by copper(I)pybox complex in water and in toluene. Wei C, Li CJ. J Am Chem Soc; 2002 May 22; 124(20):5638-9. PubMed ID: 12010027 [Abstract] [Full Text] [Related]
20. 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] Page: [Next] [New Search]