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Angewandte Chemie (International ed.), ISSN 1433-7851, 2017, Volume 56, Issue 27, pp. 7720 - 7738
Journal Article
Chemistry, an Asian journal, ISSN 1861-4728, 2018, Volume 13, Issue 9, pp. 1089 - 1102
Pentamethylcyclopentadienyl (Cp*)‐based Group 9 metal (Co, Rh, or Ir) catalysts have emerged as powerful tools for C−H functionalization reactions. Whilst a... 
C−H functionalization | iridium | reaction mechanisms | cobalt | rhodium
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2013, Volume 52, Issue 31, pp. 8031 - 8036
New horizons in the utility of azides: The rhodium‐catalyzed intermolecular direct CH amination of arenes with alkyl azides provides a convenient route to... 
alkyl nitrenoids | CH amination | azides | rhodium catalysis | aniline derivatives | C-H amination | Utilities | Ketones | Rhodium | Aniline | Aromatic compounds | Catalysis | Benzamide | Functional groups
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 2013, Volume 19, Issue 23, pp. 7328 - 7333
CH activation: The ruthenium‐catalyzed direct sp2 CH amidation of arenes by using sulfonyl azides as the amino source is presented (see scheme). A wide range... 
ruthenium | catalysis | CH activation | amination | sulfonyl azides | C-H activation | Alkenes - chemistry | Azides | Heterocyclic Compounds - chemistry | Hydrogen Bonding | Ketones - chemistry | Heterocyclic Compounds - chemical synthesis | Catalysis | Ruthenium - chemistry | Utilities | Activation | Ketones | Aromatic compounds | Bearing
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2015, Volume 54, Issue 47, pp. 14103 - 14107
A procedure for the [Cp*CoIII]‐catalyzed direct CH amidation of arenes with dioxazolone has been developed. This reaction proceeds under straightforward and... 
amidation | CH activation | dioxazolones | cobalt catalysis | anilides | C-H activation | AMINO SOURCES | ACTIVATION | AZIDES | CYANATION | COPPER | CHEMISTRY, MULTIDISCIPLINARY | (HETERO)ARENES | MILD | FUNCTIONALIZATION | AMINATION | N BOND FORMATION
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 08/2017, Volume 23, Issue 46, pp. 11147 - 11152
Described herein is a mechanism‐based approach to develop a versatile C−H amidation protocol under IrIII catalysis. Reaction kinetics of a key C−N coupling... 
iridium | density functional calculations | amination | C−N coupling | transition states | Chemical reaction, Rate of | Analysis | Catalysis | Coupling (molecular) | Decarboxylation | Computer applications | Reaction kinetics | Catalytic activity | Kinetics | Nitrogen | Substrates
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2014, Volume 53, Issue 8, pp. 2203 - 2207
An iridium‐catalyzed direct CH amidation of weakly coordinating substrates, in particular of those bearing ester and ketone groups, under very mild conditions... 
iridium | CH amidation | esters | azides | weakly coordinating groups | C-H amidation | PALLADIUM | ARENES | COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | AMINATION | OLEFINATION | BOND ACTIVATION | INHIBITORS | EFFICIENT | Additives | Ketones | Esters | Lithium carbonate | Acetic acid | Carbonyls | Bearing
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2016, Volume 55, Issue 5, pp. 1876 - 1880
New reactivity of a [Cu(NHC)] (NHC=N‐heterocyclic carbene) catalyst is disclosed for the efficient C−H allylation of polyfluoroarenes using allyl halides in... 
copper | alkenes | isomerization | allylic compounds | N-heterocyclic carbenes | CATALYZED ISOMERIZATION | ARYLATION | BOND FUNCTIONALIZATION | AROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | ARYL BROMIDES | MILD | OLEFINS | Halides | Isomerization | Stereoselectivity | Catalysts | Aromatic compounds | Temperature effects | Benzene | Migration | Tetrahydrofuran | Chemical reactions | Allyl compounds | Substrates
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2017, Volume 56, Issue 15, pp. 4256 - 4260
Polyaminobenzenes were synthesized by the ruthenium‐catalyzed iterative C−H amidation of anilides using dioxazolones as an amino source. This strategy could be... 
amidation | reaction mechanisms | ruthenium | C−H activation | arenes | AROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | AMINATION | C-H activation | SULFONYL AZIDES | AMIDO TRANSFER | NITROGEN-SOURCE | BOND ACTIVATION | CATALYZED 4+2 BENZANNULATION | DERIVATIVES | CHELATION ASSISTANCE | Chelation | Amides | Ruthenium | Computer applications
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2017, Volume 56, Issue 9, pp. 2408 - 2412
A change in reaction pathway was achieved for the first time by tuning the cyclopentadienyl (Cp) ligand used for the rhodium‐catalyzed cyclization of... 
cyclopentadienyl ligands | reaction mechanisms | annulations | rhodium catalysis | Rhodium
Journal Article