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Advanced Synthesis & Catalysis, ISSN 1615-4150, 10/2017, Volume 359, Issue 19, pp. 3274 - 3291
The one‐step direct regioselective functionaliztion of inert C(sp2)–H bonds is an efficient and sustainable methodology for the synthesis of a variety of... 
nitriles | directing group | C–H functionalization | arylation | olefination | ARENES | CHEMISTRY, ORGANIC | C-H functionalization | U-SHAPED TEMPLATE | CYANO | BIDENTATE | BOND ACTIVATION | ARYLNITRILES | CHEMISTRY, APPLIED | BORYLATION | AROMATIC NITRILES | Nitriles | Ruthenium | Rhodium | Hydroxylation | Hydrogen bonds | Natural products | Halogenation | Palladium | Iridium | Functional groups | Ruthenium compounds | Carbonyls
Journal Article
Journal of Organometallic Chemistry, ISSN 0022-328X, 08/2016, Volume 815-816, pp. 59 - 64
A mild and efficient substrate-assisted C-H bond cyanation of 2-arylbenzothiazoles has been developed using CuCN as cyano-group source. The reaction exhibits... 
Cyanation | 2-Arylbenzothiazoles | Substrate-assisted | DIRECTING GROUP | BENZOTHIAZOLE | ACTIVATION | CHEMISTRY, ORGANIC | CHEMISTRY, INORGANIC & NUCLEAR | FUNCTIONALIZATION | U-SHAPED TEMPLATE | OLEFINATION | COUPLING REACTIONS | ARYL HALIDES | ORTHO-ACYLATION | DERIVATIVES | Nitriles
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2017, Volume 23, Issue 48, pp. 11519 - 11523
The first example of meta‐selective C−H arylations of arene alcohol‐based substrates is described. The strategy involves the combination of the transient... 
palladium | alcohols | molecular scaffold | biaryls | C−H arylation | DIRECTING GROUP | ACTIVATION | MASKED BENZYL ALCOHOLS | ALKYLATION | ARENES | BOND FUNCTIONALIZATION | C-H arylation | PD/NORBORNENE | CHEMISTRY, MULTIDISCIPLINARY | PHENYLACETIC ACIDS | U-SHAPED TEMPLATE | OLEFINATION | Quinoline | Telescoping | Alcohol | Catalysis | Substrates | Alcohols | meta-C-H arylation | quinoline acetal
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 03/2017, Volume 2017, Issue 9, pp. 1239 - 1252
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 12/2016, Volume 358, Issue 24, pp. 3932 - 3937
An inexpensive ruthenium‐catalyzed direct C–H olefination of aromatic carboxamides with allyl acetate was developed. This external oxidant‐free protocol... 
cross-coupling | ruthenium | allyl acetate | styrenes | olefination | CATALYSIS | FUNCTIONALIZATIONS | ELECTRON-DEFICIENT POLYFLUOROARENES | ARENES | CHEMISTRY, ORGANIC | ALKYNES | ALKENES | U-SHAPED TEMPLATE | BOND ACTIVATION | CHEMISTRY, APPLIED | HECK REACTION | ALKENYLATION | Acetates | Ruthenium | Nitrogen dioxide | Functional groups | Ruthenium compounds | Synthesis (chemistry) | Synthesis | Derivatives | Catalysis
Journal Article
Synlett, ISSN 0936-5214, 01/2016, Volume 27, Issue 2, pp. 277 - 281
Abstract While a great number of ortho C–H functionalization reactions have been developed and several breakthroughs have been achieved in meta C–H activation,... 
letter | palladium | regio-selectivity | C-H activation | decarboxylation | arenes | regioselectivity | DIRECTING GROUP | META | BOND FUNCTIONALIZATION | CHEMISTRY, ORGANIC | ARYL ETHERS | PHENOL DERIVATIVES | DIRECT ORTHO-ARYLATION | CROSS-COUPLING REACTIONS | U-SHAPED TEMPLATE | SELECTIVE ARYLATION | CARBOXYLIC-ACIDS
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 11/2015, Volume 21, Issue 48, pp. 17474 - 17478
Biaryls, which contained a benzyloxy motif, were directly constructed through a ligand‐promoted PdII‐catalyzed ortho‐arylation of masked aromatic alcohols. A... 
CH activation | alcohols | cross‐coupling | synthetic methods | arylation | cross-coupling | C-H activation | C(SP)-H BONDS | ENANTIOSELECTIVE SYNTHESIS | AMINO-ACID LIGANDS | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | ACTIVATION/C-O CYCLIZATION | U-SHAPED TEMPLATE | ARYLBORON REAGENTS | BORON REAGENTS | PD CATALYSTS | Palladium | Hydroxides | Synthesis | Biocompatibility | Esters | Joining | Derivatives | Catalysis | Ethers | Alcohols
Journal Article
ChemCatChem, ISSN 1867-3880, 08/2016, Volume 8, Issue 15, pp. 2472 - 2475
We report a new strategy for the synthesis of phenols from acyclic unsaturated ketones in one pot. The reaction proceeds by palladium‐catalyzed... 
oxidation | palladium | phenol | Phenol | Oxidation | Palladium | DIRECTING GROUP | ORGANIC-CHEMICALS | C-H OLEFINATION | CHEMISTRY, PHYSICAL | SUBSTITUTED CYCLOHEXANONES | UNACTIVATED OLEFINS | UNSATURATED-KETONES | U-SHAPED TEMPLATE | BETA-DIKETONES | INTRAMOLECULAR HYDROALKYLATION | AEROBIC DEHYDROGENATION
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 08/2016, Volume 2016, Issue 22, pp. 3679 - 3683
Catechol mono‐ethers are an important class of phenols. They are found in a number of pharmaceuticals, flavoring agents, perfumes, and are used for the... 
C–H substitution | Oxidative dearomatization | Regioselectivity | Alkylation | Radicals | DIRECTING GROUP | C-H substitution | DIRECT ARYLATION | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | RADICAL-ADDITION | ORGANOBORANES | PHENOL DERIVATIVES | U-SHAPED TEMPLATE | OLEFINATION | ORTHOQUINONE MONOKETALS | DEAROMATIZATION | Flavoring essences
Journal Article
Synlett, ISSN 0936-5214, 09/2016, Volume 27, Issue 14, pp. 2043 - 2050
Abstract A ligand-controlled discovery of ortho and meta C–H boryl­ation of aromatic aldehydes is described. In both cases, an amine is used and it was... 
synpacts | ortho borylation | benzaldehyde | C-H activation | meta borylation | iridium catalyst | ACID | CATALYZED REACTIONS | CHEMISTRY, ORGANIC | DIRECTED ORTHO BORYLATION | PHENOL DERIVATIVES | U-SHAPED TEMPLATE | BROMINATION | OLEFINATION | BOND ACTIVATION | SUPPORTED IRIDIUM COMPLEX | FUNCTIONALIZED ARENES
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 09/2016, Volume 22, Issue 37, pp. 13054 - 13058
Journal Article