Mechanistic Insights into the One-Pot Synthesis of Propargylamines from Terminal Alkynes and Amines in Chlorinated Solvents Catalyzed by Gold Compounds and Nanoparticles

被引:65
作者
Aguilar, David [3 ]
Contel, Maria [1 ,2 ]
Urriolabeitia, Esteban P. [3 ]
机构
[1] CUNY, Brooklyn Coll, Dept Chem, Brooklyn, NY 11210 USA
[2] CUNY, Grad Ctr, Brooklyn, NY 11210 USA
[3] Univ Zaragoza, CSIC, Inst Ciencia Mat Aragon, Dept Compuestos Organometal, E-50009 Zaragoza, Spain
关键词
alkynes; C-C coupling; C-Cl activation; catalysis; gold; 3-COMPONENT COUPLING REACTION; DICHLOROMETHANE ACTIVATION; IMINOPHOSPHORANE COMPLEXES; BOND ACTIVATION; DIRECT-ADDITION; ALDEHYDE; COPPER; SILVER; 2,3,4,5-TETRAHYDROPYRIDINES; 5-ALKYNYLAMINES;
D O I
10.1002/chem.201000587
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Propargylamines can be obtained from secondary amines and terminal alkynes in chlorinated solvents by a three- and two-component synthesis catalyzed by gold compounds and nanoparticles (Au-NP) under mild conditions. The use of dichloromethane allows for the activation of two C-Cl bonds and a clean transfer of the methylene fragment to the final product. The scope of the reaction as well as the influence of different gold(III) cycloaurated complexes and salts has been investigated. The involvement of gold nanoparticles generated in situ in the process is discussed and a plausible reaction mechanism is proposed on the basis of the data obtained.
引用
收藏
页码:9287 / 9296
页数:10
相关论文
共 78 条
[31]   A simple large-scale synthesis of nearly monodisperse gold and silver nanoparticles with adjustable sizes and with exchangeable surfactants [J].
Hiramatsu, H ;
Osterloh, FE .
CHEMISTRY OF MATERIALS, 2004, 16 (13) :2509-2511
[32]   A monometallic Rh(III) tetraphosphine complex:: Reductive activation of CH2Cl2 and selective meso to racemic tetraphosphine ligand isomerization [J].
Hunt, C ;
Fronczek, FR ;
Billodeaux, DR ;
Stanley, GG .
INORGANIC CHEMISTRY, 2001, 40 (20) :5192-5198
[33]  
JANDIK P, 1982, ANGEW CHEM, V94, P74
[34]   Highly enantioselective construction of fused pyrrolidine systems that contain a quaternary stereocenter: Concise formal synthesis of (+)-conessine [J].
Jiang, B ;
Xu, M .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (19) :2543-2546
[35]  
Jiang B., 2004, ANGEW CHEM, V116, P2597
[36]   Gold-catalyzed cycloisomerizations of enynes:: A mechanistic perspective [J].
Jimenez-Nunez, Eloisa ;
Echavarren, Antonio M. .
CHEMICAL REVIEWS, 2008, 108 (08) :3326-3350
[37]   Layered double hydroxide-supported gold catalyst for three-component aldehyde-amine-alkyne coupling [J].
Kantam, ML ;
Prakash, BV ;
Reddy, CRV ;
Sreedhar, B .
SYNLETT, 2005, (15) :2329-2332
[38]   The first Au-nanoparticles catalyzed green synthesis of propargylamines via a three-component coupling reaction of aldehyde, alkyne and amine [J].
Kidwai, Mazaahir ;
Bansal, Vikas ;
Kumar, Ajeet ;
Mozumdar, Subho .
GREEN CHEMISTRY, 2007, 9 (07) :742-745
[39]   LEAVING GROUP SELECTIVITY IN REDUCTIVE ELIMINATION FROM ORGANOGOLD(III) COMPLEXES [J].
KOMIYA, S ;
OZAKI, S ;
SHIBUE, A .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1986, (20) :1555-1556
[40]   Synthesis of enantiomerically enriched propargylamines by copper-catalyzed addition of alkynes to enamines [J].
Koradin, C ;
Gommermann, N ;
Polborn, K ;
Knochel, P .
CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (12) :2797-2811