A novel catalyst Pd@ompg-C3N4 for highly chemoselective hydrogenation of quinoline under mild conditions
暂无分享,去创建一个
Yong Wang | Haoran Li | Pengfei Zhang | Xuan Xu | Yutong Gong | Yi Li
[1] Belinda S. Akpa,et al. Solvent effects in the hydrogenation of 2-butanone , 2012 .
[2] Yong Wang,et al. Polymeric graphitic carbon nitride as a heterogeneous organocatalyst: from photochemistry to multipurpose catalysis to sustainable chemistry. , 2012, Angewandte Chemie.
[3] Merlín Rosales,et al. Kinetics and Mechanisms of Homogeneous Catalytic Reactions. Part 11. Regioselective Hydrogenation of Quinoline Catalyzed by Rhodium Systems Containing 1,2-Bis(diphenylphosphino)ethane , 2011 .
[4] M. Antonietti,et al. Visible‐Light‐Induced Metal‐Free Allylic Oxidation Utilizing a Coupled Photocatalytic System of g‐C3N4 and N‐Hydroxy Compounds , 2011 .
[5] B. Shi,et al. Catalytic hydrogenation of quinoline over recyclable palladium nanoparticles supported on tannin grafted collagen fibers , 2011 .
[6] Scott J. Miller,et al. Iridium-catalyzed hydrogenation of N-heterocyclic compounds under mild conditions by an outer-sphere pathway. , 2011, Journal of the American Chemical Society.
[7] M. Antonietti,et al. Highly selective hydrogenation of phenol and derivatives over a Pd@carbon nitride catalyst in aqueous media. , 2011, Journal of the American Chemical Society.
[8] M. Antonietti,et al. Synthesis of boron doped polymeric carbon nitride solids and their use as metal-free catalysts for aliphatic C–H bond oxidation , 2011 .
[9] E. Haque,et al. Superior adsorption capacity of mesoporous carbon nitride with basic CN framework for phenol , 2010 .
[10] J. Figueiredo,et al. Oxygen activation sites in gold and iron catalysts supported on carbon nitride and activated carbon , 2010 .
[11] M. Antonietti,et al. Excellent Visible-Light Photocatalysis of Fluorinated Polymeric Carbon Nitride Solids , 2010 .
[12] K. Jitsukawa,et al. Fine Tuning of Pd0 Nanoparticle Formation on Hydroxyapatite and Its Application for Regioselective Quinoline Hydrogenation , 2010 .
[13] M. Antonietti,et al. Boron- and fluorine-containing mesoporous carbon nitride polymers: metal-free catalysts for cyclohexane oxidation. , 2010, Angewandte Chemie.
[14] M. Antonietti,et al. Mesoporous, 2D Hexagonal Carbon Nitride and Titanium Nitride/Carbon Composites , 2009 .
[15] A. Vinu,et al. Highly ordered mesoporous carbon nitride nanoparticles with high nitrogen content: a metal-free basic catalyst. , 2009, Angewandte Chemie.
[16] M. Antonietti,et al. Ordered Mesoporous SBA-15 Type Graphitic Carbon Nitride: A Semiconductor Host Structure for Photocatalytic Hydrogen Evolution with Visible Light , 2009 .
[17] Yanmei He,et al. Highly enantioselective hydrogenation of quinolines under solvent-free or highly concentrated conditions , 2009 .
[18] K. Fujita,et al. Homogeneous catalytic system for reversible dehydrogenation-hydrogenation reactions of nitrogen heterocycles with reversible interconversion of catalytic species. , 2009, Journal of the American Chemical Society.
[19] K. Okano,et al. A mild inter- and intramolecular amination of aryl halides with a combination of CuI and CsOAc , 2008 .
[20] R. Schlögl,et al. Graphitic carbon nitride materials: variation of structure and morphology and their use as metal-free catalysts , 2008 .
[21] K. Wilson,et al. The influence of surface functionalization of activated carbon on palladium dispersion and catalytic activity in hydrogen oxidation , 2008 .
[22] R. Sánchez-Delgado,et al. Hydrogenation of quinoline by ruthenium nanoparticles immobilized on poly(4-vinylpyridine). , 2007, Catalysis communications.
[23] Yong‐Gui Zhou. Asymmetric hydrogenation of heteroaromatic compounds. , 2007, Accounts of chemical research.
[24] Xiuwen Han,et al. An efficient catalytic system for the hydrogenation of quinolines , 2007 .
[25] V. Dubois,et al. Nanostructured Pd/C catalysts prepared by grafting of model carboxylate complexes onto functionalized carbon , 2006 .
[26] M. Vannice,et al. Solvent effects in liquid-phase reactions: I. Activity and selectivity during citral hydrogenation on Pt/SiO2 and evaluation of mass transfer effects , 2006 .
[27] M. Antonietti,et al. Chemical synthesis of mesoporous carbon nitrides using hard templates and their use as a metal-free catalyst for Friedel-Crafts reaction of benzene. , 2006, Angewandte Chemie.
[28] Xiuwen Han,et al. Asymmetric Hydrogenation of Quinolines Catalyzed by Iridium with Chiral Ferrocenyloxazoline Derived N,P Ligands , 2004 .
[29] L. Kiwi-Minsker,et al. Highly dispersed gold on activated carbon fibers for low-temperature CO oxidation , 2004 .
[30] Merlín Rosales,et al. Kinetics and mechanisms of homogeneous catalytic reactions. Part 5. Regioselective reduction of heteroaromatic nitrogen compounds catalysed by [OsH(CO)(NCMe)2(PPh3)2]BF4 , 2004 .
[31] Xiuwen Han,et al. Highly enantioselective iridium-catalyzed hydrogenation of heteroaromatic compounds, quinolines. , 2003, Journal of the American Chemical Society.
[32] A. Spitaleri,et al. Supported ruthenium nanoparticles on polyorganophosphazenes: preparation, structural and catalytic studies , 2003 .
[33] R. Schneider,et al. Efficient nickel-mediated intramolecular amination of aryl chlorides. , 2003, Organic letters.
[34] A. Vaccari,et al. Mild hydrogenation of quinoline: 2. A novel Rh-containing pillared layered clay catalyst , 2002 .
[35] A. Vaccari,et al. Mild hydrogenation of quinoline: 1. Role of reaction parameters , 2002 .
[36] M. Busolo,et al. Regioselective homogeneous hydrogenation of quinoline by use of pyrazolyl borate ligand and transition metal complexes as a precatalyst , 1999 .
[37] Bradley F. Chmelka,et al. Nonionic Triblock and Star Diblock Copolymer and Oligomeric Surfactant Syntheses of Highly Ordered, Hydrothermally Stable, Mesoporous Silica Structures , 1998 .
[38] A. Katritzky,et al. Recent progress in the synthesis of 1,2,3,4,-tetrahydroquinolines , 1996 .
[39] B. Chaudret,et al. Kinetics and mechanism of the regioselective homogeneous hydrogenation of quinoline using [Rh(COD)(PPh3)2]PF6 as the catalyst precursor , 1993 .
[40] I. Horváth,et al. Homogeneous catalytic hydrogenation. 6. Synthetic and mechanistic aspects of the regioselective reductions of model coal nitrogen, sulfur, and oxygen heteroaromatic compounds using the (.eta.5-pentamethylcyclopentadienyl)rhodium tris(acetonitrile) dication complex as the catalyst precursor , 1992 .
[41] H. Kim,et al. Bonding of mono- and polynuclear heteroaromatic nitrogen ligands to the (.eta.5-pentamethylcyclopentadienyl)rhodium dication: structure-reactivity relationships in the formation of nitrogen (.eta.1) versus .pi.(.eta.5,.eta.6) complexes and competition studies of the ligands for the rhodium metal cen , 1991 .
[42] J. N. Michaels,et al. Gas-phase hydrodenitrogenation reactions of polynuclear heteroaromatic nitrogen compounds and selected intermediates with a 50% nickel oxide/aluminate supported on s silica-alumina catalyst*1 , 1990 .
[43] R. Taft,et al. Solvent effects in organic chemistry — recent developments , 1988 .
[44] T. Miyazaki,et al. Organoaluminum-promoted Beckmann rearrangement of oxime sulfonates , 1983 .
[45] R. Fish,et al. Homogeneous catalytic hydrogenation. 1. Regiospecific reductions of polynuclear aromatic and polynuclear heteroaromatic nitrogen compounds catalyzed by transition metal carbonyl hydrides , 1982 .
[46] V. Likholobov,et al. Palladium catalysts on activated carbon supports: Influence of reduction temperature, origin of the support and pretreatments of the carbon surface , 2000 .
[47] P. Ornstein,et al. An improved synthesis of homoproline and derivatives , 1990 .
[48] R. A. Rajadhyaksha,et al. Solvent effects in catalytic hydrogenation , 1986 .