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Angewandte Chemie International Edition, ISSN 1433-7851, 03/2016, Volume 55, Issue 12, pp. 4040 - 4043
Journal Article
Chemical Reviews, ISSN 0009-2665, 08/2018, Volume 118, Issue 16, pp. 7532 - 7585
Transition metal-catalyzed C–H bond functionalizations have been the focus of intensive research over the last decades for the formation of C–C bonds from... 
H FUNCTIONALIZATION | ROOM-TEMPERATURE | DIRECT ARYLATION | ARYL DIAZONIUM SALTS | VISIBLE-LIGHT PHOTOREDOX | PYRIDINE N-OXIDES | SINGLE-ELECTRON TRANSMETALATION | MEDIATED RADICAL ARYLDIFLUOROACETYLATION | CHEMISTRY, MULTIDISCIPLINARY | METAL-FREE | CARBOXYLIC-ACIDS | Chemical Sciences
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
The Journal of Organic Chemistry, ISSN 0022-3263, 08/2016, Volume 81, Issue 16, pp. 6898 - 6926
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2019, Volume 58, Issue 7, pp. 2139 - 2143
Under mild dual photoredox/copper catalysis, the reaction of N‐alkoxypyridinium salts with readily available silyl reagents (TMSN3, TMSCN, TMSNCS) afforded... 
alkoxy radical | C−H activation | dual catalysis | photoredox catalyst | 1,5-HAT | 5-HAT | DECOMPOSITION | HYDROGEN-ATOM | COPPER | CHEMISTRY, MULTIDISCIPLINARY | ALKENES | C-H activation | BONDS | ALKOXYL RADICALS | GENERATION | RELAY CYCLIZATIONS | METAL-FREE | CHLORINATION | Salts | Halides | Reagents | Alcohol | Catalysis | Copper | Enantiomers | Alcohols
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2017, Volume 359, Issue 11, pp. 1976 - 1980
A simple and efficient protocol for the iron(III)‐catalyzed C5 halogenation of 8‐aminoquinoline with potassium halides via a photoredox process was developed,... 
iron(III) catalysis | photoredox catalysis | bromination and iodination | water | 8-aminoquinoline | HALIDES | ORGANIC-SYNTHESIS | CHEMISTRY, ORGANIC | HALOGENATION | BIFUNCTIONAL ORGANOCATALYSTS | FUNCTIONALIZATION | VISIBLE-LIGHT | MILD CONDITIONS | COUPLING REACTIONS | BONDS | CHEMISTRY, APPLIED | Amides | Catalysis | Iodination | Bromination | Halides | Halogenation | Iron | Potassium | Substrates
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, 04/2012, Volume 51, Issue 17, pp. 4144 - 4147
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