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1. Full Text On‐Surface Reactions
by Lindner, Robert and Kühnle, Angelika
ChemPhysChem, ISSN 1439-4235, 06/2015, Volume 16, Issue 8, pp. 1582 - 1592
On‐surface synthesis constitutes a rapidly growing field of research due to its promising application for creating stable molecular structures on surfaces.... 
two‐dimensional confinement | ultrahigh vacuum | molecular electronics | scanning probe microscopy | molecular structure formation | Molecular structure formation | Molecular electronics | Scanning probe microscopy | Two-dimensional confinement | Ultrahigh vacuum | two-dimensional confinement | AZIDE-ALKYNE CYCLOADDITION | CATALYZED CYCLODEHYDROGENATION | AROMATIC PRECURSORS | MOLECULAR BUILDING-BLOCKS | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | CHEMISTRY, PHYSICAL | ULLMANN POLYMERIZATION | COVALENT ORGANIC FRAMEWORKS | BULK INSULATOR | SCANNING-TUNNELING-MICROSCOPY | METAL-SURFACES | ULTRAHIGH-VACUUM
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2. Full Text Synthesis of N‑(α-Fluorovinyl)azoles by the Reaction of Difluoroalkenes with Azoles
by Xiong, Yang and Zhang, Xuxue and Huang, Tao and Cao, Song
The Journal of Organic Chemistry, ISSN 0022-3263, 07/2014, Volume 79, Issue 14, pp. 6395 - 6402
A mild and versatile method for the construction of C–N bonds by the reaction of (2,2-difluorovinyl)arenes with various N–H-containing heterocycles in the... 
NITROGEN-CONTAINING HETEROCYCLES | ARYL BROMIDES | CATALYZED N-ARYLATION | INTRAMOLECULAR CYCLIZATION | DIPEPTIDYL-PEPTIDASE-IV | CROSS-COUPLING REACTION | NUCLEOPHILIC 5-ENDO-TRIG CYCLIZATION | C-N | CHEMISTRY, ORGANIC | ULLMANN-TYPE REACTION | VINYL BROMIDES | Azoles - chemistry | Hydrocarbons, Fluorinated - chemical synthesis | Heterocyclic Compounds - chemical synthesis | Hydrocarbons, Fluorinated - chemistry | Molecular Structure | Heterocyclic Compounds - chemistry | Azoles (Class of compounds) | Chemical properties | Research | Structure | Chemical synthesis | Olefins
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3. Full Text An Ullmann CO Coupling Reaction Catalyzed by Magnetic Copper Ferrite Nanoparticles
by Yang, Shuliang and Wu, Cunqi and Zhou, Hua and Yang, Yanqin and Zhao, Yongxia and Wang, Chenxu and Yang, Wei and Xu, Jingwei
Advanced Synthesis & Catalysis, ISSN 1615-4150, 01/2013, Volume 355, Issue 1, pp. 53 - 58
Herein, an efficient method for the Ullmann CO coupling reaction between various kinds of phenols and aryl halides, including amino, ketone, cyano, methyl,... 
catalyst recycling | copper ferrite (CuFe2O4) | Ullmann reaction | magnetic particles | CO cross‐coupling | C-O cross-coupling | copper ferrite (CuFe | POTASSIUM TERT-BUTOXIDE | CHEMISTRY, ORGANIC | C?O cross-coupling | BOND FORMATION | EFFICIENT CATALYST | MILD CONDITIONS | PHENOLS | VERSATILE | DIARYL ETHER FORMATION | ARYL HALIDES | CHEMISTRY, APPLIED | N-ARYLATION | NITROGEN LIGANDS | Nanoparticles | PARTICLES | FERRITE | Derivatives | Recycled | Copper | JOINING | CATALYSTS | CU
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4. Full Text CuI/Oxalic Diamide Catalyzed Coupling Reaction of (Hetero)Aryl Chlorides and Amines
by Zhou, Wei and Fan, Mengyang and Yin, Junli and Jiang, Yongwen and Ma, Dawei
Journal of the American Chemical Society, ISSN 0002-7863, 09/2015, Volume 137, Issue 37, pp. 11942 - 11945
A class of oxalic diamides are found to be effective ligands for promoting CuI-catalyzed aryl amination with less reactive (hetero)­aryl chlorides. The... 
ROOM-TEMPERATURE | AMINATION | C-N | ARYL HALIDES | EFFICIENT COPPER CATALYST | BOND FORMATION | ULLMANN REACTION | LIGAND | N-ARYLATION | CONTAINING HETEROCYCLES | CHEMISTRY, MULTIDISCIPLINARY | Amines - chemistry | Copper - chemistry | Oxalic Acid - chemistry | Chlorine - chemistry | Diamide - chemistry | Iodides - chemistry | Catalysis | Ligands | Aromatic amines | Research
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5. Full Text Copper in cross-coupling reactions: The post-Ullmann chemistry
by Beletskaya, Irina P and Cheprakov, Andrei V
Coordination Chemistry Reviews, ISSN 0010-8545, 12/2004, Volume 248, Issue 21-24, pp. 2337 - 2364
In the last decade, a number of methods using various copper complexes and salts to carry out cross-coupling reactions leading to the formation of Cheteroatom... 
Cross-coupling | Catalysis | Copper | Ullmann reaction | CATALYZED N-ARYLATION | IODIDE-PROMOTED ALLYLATION | SALICYLIC-ACID DERIVATIVES | catalysis | AROMATIC NUCLEOPHILIC-SUBSTITUTION | CHEMISTRY, INORGANIC & NUCLEAR | DIARYL ETHER SYNTHESIS | ORTHO C-CL | cross-coupling | 2-CARBOXY SUBSTITUTED DIPHENYLETHERS | copper | UNACTIVATED ARYL HALIDES | GRIGNARD-REAGENTS | MIZOROKI-HECK TYPE
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6. Full Text Kinetic Investigation of a Ligand‐Accelerated Sub‐mol % Copper‐Catalyzed CN Cross‐Coupling Reaction
by Larsson, Per‐Fredrik and Bolm, Carsten and Norrby, Per‐Ola and Institutionen för kemi and Naturvetenskapliga fakulteten and Faculty of Sciences and Department of Chemistry and Göteborgs universitet and Gothenburg University
Chemistry – A European Journal, ISSN 0947-6539, 12/2010, Volume 16, Issue 46, pp. 13613 - 13616
Unique ligand acceleration: A kinetic investigation of the copper‐catalyzed CN cross‐coupling in the sub‐mol % range reveals an exceptional ligand dependence.... 
copper | ligand acceleration | cross‐coupling | kinetics | sub‐mol % catalysis | cross-coupling | sub-mol % catalysis | HALIDES | sub-mol% catalysis | ARYLATION | COMPLEXES | AMIDATION | IMIDAZOLES | CHEMISTRY, MULTIDISCIPLINARY | DIAMINE LIGANDS | NUCLEOPHILES | ARYL IODIDES | EFFICIENT | ULLMANN | Pyrazoles - chemistry | Copper - chemistry | Cross-Linking Reagents - chemistry | Ligands | Molecular Structure | Catalysis | Kinetics | Cross coupling | Low concentrations | Catalysts | Reaction kinetics | Chemical reactions | Copper | Acceleration | Kemi | Chemical Sciences
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7. Full Text Diamine ligands in copper-catalyzed reactions
by Surry, David S and Buchwald, Stephen L
Chemical Science, ISSN 2041-6520, 6/2010, Volume 1, Issue 1, pp. 13 - 31
The utility of copper-mediated cross-coupling reactions has been significantly increased by the development of mild reaction conditions and the ability to... 
NITROGEN-CONTAINING HETEROCYCLES | CROSS-COUPLING REACTIONS | ULLMANN-TYPE SYNTHESIS | AMINO-ACID | SULFINIC ACID SALTS | DIPEPTIDYL-PEPTIDASE-IV | C-N | ARYL HALIDES | N BOND FORMATION | HIGHLY EFFICIENT SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY
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8. Full Text New Perspectives on Classical Heterocyclic Reactions Involving Pyrrole Derivatives (Review)
by Yurovskaya, M A and Alekseyev, R S
Chemistry of Heterocyclic Compounds, ISSN 0009-3122, 1/2014, Volume 49, Issue 10, pp. 1400 - 1425
Our review concerns the classical heterocyclic name reactions of pyrrole derivatives that were discovered in late 19th and early 20th centuries, and... 
Brunner reaction | indole | Madelung reaction | Bischler–Möhlau reaction | carboline | pyrrole | Knorr reaction | Nenitzescu reaction | Chemistry | Pharmacy | Graebe–Ullmann reaction | carbazole | Hantzsch reaction | Organic Chemistry | Piloty–Robinson reaction | Piloty-Robinson reaction | Graebe-Ullmann reaction | Bischler-Möhlau reaction | MODIFIED MADELUNG REACTION | SOLID-PHASE SYNTHESIS | SUBSTITUTED PYRROLES | ALPHA-CARBOLINE | GAMMA-CARBOLINES | CHEMISTRY, ORGANIC | REAKTSII PROIZVODNYKH GIDRAZINA | SYNTHETIC UTILITY | INDOLE SYNTHESIS | Bischler-Mohlau reaction | Heterocyclic compounds | Thiophene
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9. Full Text Ordered Mesoporous Pd/Silica−Carbon as a Highly Active Heterogeneous Catalyst for Coupling Reaction of Chlorobenzene in Aqueous Media
by Wan, Ying and Wang, Haiyan and Zhao, Qingfei and Klingstedt, Miia and Terasaki, Osamu and Zhao, Dongyuan and Stockholms universitet and Naturvetenskapliga fakulteten and Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi
Journal of the American Chemical Society, ISSN 0002-7863, 04/2009, Volume 131, Issue 12, pp. 4541 - 4550
Heterogeneous palladium catalysts, which are supported on ordered mesoporous silica−carbon nanocomposites, have been applied in water-mediated coupling... 
NANOCOMPOSITE MATERIALS | SILICA COMPOSITE | ORGANIC-INORGANIC HYBRID | MEDIUM ULLMANN REACTION | TEMPLATING SYNTHESIS | TRANSFER HYDROGENATION | PD CATALYSTS | MOLECULAR-SIEVES | HECK REACTION | CHEMISTRY, MULTIDISCIPLINARY | PALLADIUM CATALYSTS | Chlorobenzene | Palladium catalysts | Analysis | Chemical properties | Phase transformations (Statistical physics) | Structure | Silica | Naturvetenskap | Natural Sciences
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10. Full Text Steering Surface Reaction Dynamics with a Self‐Assembly Strategy: Ullmann Coupling on Metal Surfaces
by Zhou, Xiong and Wang, Chenguang and Zhang, Yajie and Cheng, Fang and He, Yang and Shen, Qian and Shang, Jian and Shao, Xiang and Ji, Wei and Chen, Wei and Xu, Guoqin and Wu, Kai
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2017, Volume 56, Issue 42, pp. 12852 - 12856
Ullmann coupling of 4‐bromobiphenyl thermally catalyzed on Ag(111), Cu(111), and Cu(100) surfaces was scrutinized by scanning tunneling microscopy as well as... 
self-assembly strategies | surface reaction dynamics | Ullmann coupling | scanning tunneling microscopy | GRAPHENE NANORIBBONS | MACROCYCLES | POLYMERIZATION | MECHANISMS | BOTTOM | INSIGHT | CHEMISTRY, MULTIDISCIPLINARY | MONOLAYERS | RADICALS | EFFICIENCY | Scanning tunneling microscopy | Self assembly | Silver | Self-assembly | Metal surfaces | Microscopy | Coupling | Copper | Dispersion | Intermediates
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11. Full Text Organic Reactions on Silica in Water
by Minakata, Satoshi and Komatsu, Mitsuo
Chemical Reviews, ISSN 0009-2665, 02/2009, Volume 109, Issue 2, pp. 711 - 724
SUPPORTED AQUEOUS-PHASE | ASYMMETRIC TRANSFER HYDROGENATION | LEWIS-ACID CATALYSTS | PERIODIC MESOPOROUS ORGANOSILICAS | MEDIUM ULLMANN REACTION | DIELS-ALDER REACTIONS | SILYL ENOL ETHERS | IONIC LIQUID | ALLYLIC SUBSTITUTION | CHEMISTRY, MULTIDISCIPLINARY | HOMOALLYLIC ALCOHOL ISOMERIZATION | Organic Chemicals - chemical synthesis | Fluorides - chemistry | Metals - chemistry | Silicon Dioxide - chemistry | Surface Properties | Organic Chemicals - chemistry | Water - chemistry | Catalysis | Ionic Liquids - chemistry | Palladium - chemistry | Phase Transition | Hydrophobic effect | Immobilized enzymes | Chemical properties | Silica | Analysis
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12. Full Text The Role of Chelating Diamine Ligands in the Goldberg Reaction:  A Kinetic Study on the Copper-Catalyzed Amidation of Aryl Iodides
by Strieter, Eric R and Blackmond, Donna G and Buchwald, Stephen L
Journal of the American Chemical Society, ISSN 0002-7863, 03/2005, Volume 127, Issue 12, pp. 4120 - 4121
The mechanistic details of the Cu-catalyzed amidation of aryl iodides are presented. The kinetic data suggest that the diamine ligand prevents multiple... 
ULLMANN CONDENSATION | HALIDES | ORGANIC REACTIONS | SUBSTITUTION | CRYSTAL-STRUCTURE | COMPLEXES | TRIARYLAMINES | N-ARYLATION | METAL-IONS | CHEMISTRY, MULTIDISCIPLINARY | Copper - chemistry | Amides - chemical synthesis | Iodobenzenes - chemistry | Chelating Agents - chemistry | Diamines - chemistry | Ligands | Catalysis | Kinetics | Copper compounds | Aromatic compounds | Chemical properties
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13. Full Text C(sp2)−O Bond Formation through a Nickel‐Catalyzed Cross‐Coupling Reaction in Water Enabled by Micellar Catalysis
by Ahanthem, Dini and Laitonjam, Warjeet S
Asian Journal of Organic Chemistry, ISSN 2193-5807, 10/2017, Volume 6, Issue 10, pp. 1492 - 1497
A nickel‐catalyzed cross‐coupling reaction between (functionalized) aryl chlorides and alcohols that results in C(sp2)−O bond formation is described. This... 
cross-coupling | nickel | C−O bond formation | micelles | water | ROOM-TEMPERATURE | PALLADIUM | C-N | METATHESIS REACTIONS | CHEMISTRY, ORGANIC | C-O bond formation | COPPER | DIETHYL PHOSPHITE | PHENOLS | ARYL HALIDES | DIARYL ETHERS | ULLMANN
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14. Full Text An On‐Surface Reaction Confined within a Porous Molecular Template
by Judd, Chris J and Champness, Neil R and Saywell, Alex
Chemistry – A European Journal, ISSN 0947-6539, 01/2018, Volume 24, Issue 1, pp. 56 - 61
On‐surface reactions based on metal‐catalysed Ullmann coupling have been successfully employed to synthesise a wide variety of covalently coupled structures.... 
scanning probe microscopy | surface chemistry | heterogeneous catalysis | supramolecular chemistry | templated reactions | BUILDING-BLOCKS | NETWORKS | NANOSTRUCTURES | INSIGHT | CHEMISTRY, MULTIDISCIPLINARY | ULLMANN POLYMERIZATION | ORGANIZATION | CHEMISTRY | INTERMEDIATE | CHAINS | Heterogeneous catalysis | Coupling (molecular) | Vacuum | Scanning probe microscopy | Microscopy | Surface reactions | Topology | High vacuum | Substrates
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