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Angewandte Chemie International Edition, ISSN 1433-7851, 09/2017, Volume 56, Issue 40, pp. 12288 - 12291
Utilizing halogens as traceless directing goups represents an attractive strategy for C−H functionalization. A two C−H alkylation system, initiated by the... 
alkylation | palladium | C−H activation | arenes | cyclization | DOMINO REACTION | INTRAMOLECULAR ARYLATION | BIS-ANNELATED BENZENES | BOND FORMATION | N BOND | CHEMISTRY, MULTIDISCIPLINARY | DIRECTING GROUPS | FUNCTIONALIZATION | C-H activation | ARYL CHLORIDES | PROTON-ABSTRACTION MECHANISM | Palladium | Carbon-carbon composites | Halides | Halogens | Chemical bonds | Biocompatibility | Activation | Alkylation
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2017, Volume 23, Issue 48, pp. 11524 - 11528
C−H alkylations with challenging β‐hydrogen‐containing alkyl halides were accomplished with sustainable MnCl2 as the catalyst under phosphine‐ligand‐free conditions. The proximity‐induced benzamide C... 
selectivity | alkylation | C−H activation | mechanism | manganese | ACTIVATION | METHYLATION | STRATEGY | BOND FUNCTIONALIZATIONS | CARBOXAMIDES | CHEMISTRY, MULTIDISCIPLINARY | CARBON-HYDROGEN | C-H activation | NICKEL | PALLADIUM-CATALYZED ARYLATION | TRIAZOLE ASSISTANCE | ARYL | Hydrogen | Halides | Catalysts | Phosphine | Benzamide | Alkylation | Manganese
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 2016, Volume 22, Issue 22, pp. 7399 - 7402
An improved method for the reductive coupling of aryl and vinyl bromides with alkyl halides that gave high yields for a variety of substrates at room temperature with a low (2.5 to 0.5 mol... 
C−C coupling | alkenes | vinyl bromides | reductive coupling | C-C coupling | SILICON | ALLYLSILANES | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY | EPOXIDES | ALLYLIC ACETATES | ARYL HALIDES | CHLORIDES | CO-CATALYSIS | Vinyl Compounds - chemistry | Hydrocarbons, Brominated - chemistry | Molecular Structure | Catalysis | Nickel - analysis | 2,2'-Dipyridyl - chemistry | Halides | Olefins | Alkenes | Catalysts | Temperature effects | Aromatic compounds | Moisture | Bromides | Coupling | Substrates | Finishes
Journal Article
Angewandte Chemie (International ed.), ISSN 1521-3773, 2009, Volume 48, Issue 23, pp. 4114 - 4133
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 01/2017, Volume 139, Issue 2, pp. 607 - 610
A pyridine-catalyzed transition-metal-free borylation reaction of haloarenes has been developed based on the selective cross-coupling of an aryl radical and a... 
METAL-FREE BORYLATION | H BOND ACTIVATION | ROOM-TEMPERATURE | HETEROCYCLIC CARBENE BORANES | LEWIS-BASES | ARYLATION | REACTIVITY | GENERATION | ALKOXY DIBORON REAGENTS | CHEMISTRY, MULTIDISCIPLINARY | ELECTRON-TRANSFER REACTIONS | Usage | Pyridine | Aromatic amines | Chemical properties | Chemical synthesis
Journal Article