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Angewandte Chemie (International ed.), ISSN 1433-7851, 2017, Volume 56, Issue 21, pp. 5921 - 5925
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 12/2004, Volume 126, Issue 50, pp. 16433 - 16439
.... Catalysts derived from ligands 1 and 4 efficiently catalyze the coupling of electronically diverse aryl chlorides with an array of organotin reagents... 
HALIDES | MILD | EFFICIENT CATALYST | AMINATION | C-N | BOND FORMATION | ORGANOTIN REAGENTS | HECK REACTION | CHEMISTRY, MULTIDISCIPLINARY | DIRECT ALPHA-ARYLATION | GENERAL-METHOD | Ligands | Palladium | Research | Chemical properties | Catalysts
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2013, Volume 52, Issue 14, pp. 4024 - 4028
.... Arylalkynes can be coupled at various surfaces in a novel 2D Glaser coupling (see picture). This approach can be used for constructing conjugated materials directly... 
polymerization | surface chemistry | conjugation | scanning tunneling microscopy | CC coupling | C-C coupling | POLYMERS | BUILDING-BLOCKS | REACTIVITY | NETWORKS | CHEMISTRY, MULTIDISCIPLINARY | CC coupling | CHEMISTRY | FABRICATION | ULTRAHIGH-VACUUM | Polymerization | Nanotechnology | Covalence | Construction | Synthesis | Metal surfaces | Construction materials | Chemical reactions | Joining | Nanostructure
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 2017, Volume 23, Issue 52, pp. 12735 - 12738
...−C coupling of cyanides. [AsC4N4]− salts with different counterions such as [PPh4]+, [PPN]+=[Ph3P‐N‐PPh3]+, Ag+, and [BMIm]+ are reported with [BMIm][AsC4N4] being a low‐temperature ionic liquid... 
C−C coupling | arsenic | isomerization | heterocycles | cyanides | C-C coupling | MOLECULAR-STRUCTURE | TRIPLE BOND | CRYSTAL | ADDUCTS | CHEMISTRY, MULTIDISCIPLINARY | TRICYANIDE | CATIONS | NITROGEN | Arsenic | Isomerization | Cyanides | Carbon-carbon composites | Cyanide | Salts | Bismuth | Ionic liquids | Chemical bonds | Phosphorus | Antimony | Coupling | Low temperature
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2017, Volume 2017, Issue 15, pp. 2118 - 2121
...‐coupling products were obtained in moderate yields and were accompanied by the homocoupling products of the alkyl halide derivatives... 
Photoredox catalysis | C–C coupling | Nickel | Radical reactions | Cross‐coupling | Cross-coupling | C-C coupling | OXIDATION | ACTIVATION | REAGENTS | CARBON | NICKEL CATALYSIS | CHEMISTRY, ORGANIC | SINGLE-ELECTRON TRANSMETALATION | ARYL BROMIDES | SILICATES | ESTERS | VISIBLE-LIGHT-PHOTOREDOX | Organic chemistry | Chemical Sciences | Catalysis
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2013, Volume 52, Issue 9, pp. 2577 - 2580
...C coupling of arenes with aziridines by a CH activation pathway. An eight‐membered rhodacyclic intermediate resulting from the insertion of the Rh... 
aziridines | CH activation | CC coupling | rhodium | C-C coupling | C-H activation | DIRECTING GROUP | ARYLATION | OXIDATIVE ANNULATION | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | CC coupling | FUNCTIONALIZATION | EFFICIENT CATALYST | CH activation | VERSATILE | N BOND FORMATION | ARYL | ELECTRON-RICH ARENES | Insertion | Activation | Joining | Pathways | Aromatic compounds | Bonding
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2013, Volume 52, Issue 47, pp. 12430 - 12434
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2012, Volume 51, Issue 5, pp. 1252 - 1255
A breath of fresh air: The title reaction has been developed for the coupling of amines with nitroalkanes and different unmodified ketones using air as the sole oxidant under mild reaction conditions... 
gold | CH activation | air | cross‐coupling | CC coupling | C-C coupling | cross-coupling | C-H activation | ALCOHOL OXIDATION | ACTIVATION | H BOND | TERTIARY-AMINES | C?H activation | ADJACENT | CHEMISTRY, MULTIDISCIPLINARY | C?C coupling | NITROGEN ATOM | AEROBIC OXIDATION | GLYCINE DERIVATIVES | HYDROGEN-PEROXIDE | MOLECULAR-OXYGEN
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2012, Volume 51, Issue 21, pp. 5062 - 5085
Journal Article