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Angewandte Chemie International Edition, ISSN 1433-7851, 03/2016, Volume 55, Issue 12, pp. 4040 - 4043
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 10/2017, Volume 23, Issue 58, pp. 14450 - 14453
Herein we describe the auxiliary‐directed arylation of unactivated C(sp3)−H bonds with aryldiazonium salts, which proceeds under synergistic photoredox and... 
palladium | C−H activation | photoredox | metallaphotoredox | arylation | AMIDATION | CARBON-HYDROGEN BONDS | SINGLE-ELECTRON TRANSMETALATION | CHEMISTRY, MULTIDISCIPLINARY | ALIPHATIC AMIDES | C-H activation | C-H ARYLATION | NICKEL | ARYL HALIDES | OXIDATIVE CYCLIZATION | C(SP)-H | DUAL CATALYSIS | Amides | Palladium | Catalysis | Salts | Quaternary | Selectivity | Aliphatic compounds
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2018, Volume 57, Issue 32, pp. 10333 - 10337
An efficient protocol for the direct allylic C(sp3)−H bond activation of unactivated tri‐ and tetrasubstituted alkenes and their functionalization with aryl‐... 
nickel | C−H activation | alkenes | photocatalysis | allylic compounds | HALIDES | ROOM-TEMPERATURE | PALLADIUM | ARYLATION | PHOTOREDOX/NICKEL DUAL CATALYSIS | 9-MESITYL-10-METHYLACRIDINIUM | OXIDATIVE ADDITION | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY | C-H activation | ACETATES | DERIVATIVES | Olefins | Nickel | Catalysis | Alkenes | Regioselectivity | Hydrogen bonds | Aromatic compounds
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2016, Volume 55, Issue 40, pp. 12275 - 12279
Nickel can be used to promote oxidative C(sp2)−H/C(sp2)−H cross‐coupling between two heteroarenes. The reaction scope can be extended to aromatic carboxamides... 
heteroarenes | nickel | oxidative cross-coupling | homogeneous catalysis | synthetic methods | DIRECTING GROUP | AZOLES | ARYLATION | C-H ACTIVATION | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | FUNCTIONALIZATION | BONDS | DERIVATIVES | ACCESS | COBALT | Silver | Costs | Cross coupling | Functional anatomy | Chemical reactions | Nickel | Catalysis | Coupling | Compatibility | Cost engineering
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 03/2015, Volume 21, Issue 13, pp. 4962 - 4965
A novel and efficient CP bond formation reaction of diarylphosphine oxides with aryl iodides was achieved by combining nickel catalysis and... 
CP bond formation | nickel | dual catalysis | radicals | photochemistry | Dual catalysis | C-P bond formation | Nickel | Radicals | Photochemistry | GOLD | STRATEGY | PHOTOCATALYSIS | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | H ARYLATION | FUNCTIONALIZATION | CHEMISTRY | PHOSPHINE OXIDES | METAL-FREE | Iodides | Methodology | Aromatic compounds | Oxides | Tolerances | Catalysis | Bonding
Journal Article
ACS Catalysis, ISSN 2155-5435, 02/2017, Volume 7, Issue 2, pp. 1413 - 1423
Amides have been widely studied for decades, but their synthetic utility has remained limited in reactions that proceed with rupture of the amide C–N bond.... 
cross-coupling | nickel | nonprecious metal | catalysis | amides | STEREOSPECIFIC FORMATION | MERGING PHOTOREDOX | CHEMISTRY, PHYSICAL | ORGANOZINC REAGENTS | CROSS-COUPLING REACTIONS | KETONE SYNTHESIS | CARBON-NITROGEN BOND | N-C CLEAVAGE | METAL CATALYSIS | ARYL CHLORIDES | CARBOXYLIC-ACIDS
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2017, Volume 2017, Issue 15, pp. 2118 - 2121
Alkylsilicates were engaged under photoredox/nickel dual catalysis conditions with alkyl halides for the first time. The C(sp3)–C(sp3) cross‐coupling products... 
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 Edition, ISSN 1433-7851, 04/2017, Volume 56, Issue 17, pp. 4853 - 4857
para‐Selective C−H borylation of benzamides and pyridines has been achieved by cooperative iridium/aluminum catalysis. A combination of iridium catalysts... 
iridium | regioselectivity | Lewis acids | C-H activation | boronate esters | ROOM-TEMPERATURE | ARYLATION | BOND FUNCTIONALIZATION | NICKEL/LEWIS ACID CATALYSIS | CHEMISTRY, MULTIDISCIPLINARY | MONOSUBSTITUTED ARENES | PHENOLS | LIGAND | ELECTRON-RICH ARENES | DERIVATIVES | Synthesis | Pyridine | Catalysis | Organic compounds | Aluminum | Lewis acid | Pyridines | Catalysts | Regioselectivity | Aromatic compounds | Iridium | Intermediates
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 509, Issue 7500, pp. 299 - 309
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 02/2016, Volume 22, Issue 7, pp. 2236 - 2242
Journal Article
ACS Catalysis, ISSN 2155-5435, 02/2017, Volume 7, Issue 2, pp. 936 - 958
Journal Article