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01/2019, ISBN 3039212044
.... These developments cover an impressive range of catalytic N–C bond activation in electrophilic, Lewis acid, radical, and nucleophilic reaction pathways, among other transformations... 
N-heterocyclic carbene | non planar amide | ruthenium (Ru) | physical organic chemistry | gemcitabine prodrug | pyramidal amides | bridged sultams | catalysis | dipeptides | N-(1-naphthyl)acetamide | C-N ? bond cleavage | steric effects | peptide bond cleavage | transition-metal-free | palladium | N bond cleavage | N-heterocyclic carbenes (NHCs) | addition reaction | rhodium | metal complexes | carbanions | thioamidation | amide bond | intramolecular catalysis | antiviral activity | additivity principle | pre-catalysts | bridged lactams | arynes | twisted amides | organic synthesis | amination | Suzuki-Miyaura | tert-butyl | C | cyclopentadienyl complexes | C-S formation | enzymes | DFT study | sulfonamide bond | N | HERON reaction | primaquine | entropy | amide activation | amidation | synthesis | amide hydrolysis | carbonylicity | amide bond activation | amide bond resonance | aminosulfonylation | molecular dynamics | model compound | in situ | amide | homogeneous catalysis | heterocycles | anomeric effect | multi-component coupling reaction | kinetic | excited state | H acidity | palladium catalysis | amides | thiourea | formylation | alkynes | cis/trans isomerization | intein | C-H functionalization | succindiamide | amide C | amide bonds | O activation | crown ether | aminoacylation | directing groups | cytostatic activity | reaction thermodynamics | acyl transfer | transition metals | N-dimethylformamide | DMAc | acylative cross-coupling | C activation | C-H/C-N activation | nickel catalysis | antibacterial screening | sodium | aryl thioamides | Winkler-Dunitz parameters | catalyst | N-dimethylacetamide | base-catalyed hydrolysis | nitrogen heterocycles | cross-coupling | insertion | amidicity | nitro-aci tautomerism | activation | carbonylation | transamidation | amine | distortion | Pd-catalysis | rotational barrier energy | hypersensitivity | metabolic stability | [2+2+2] annulation | H bond cleavage | twisted amide | protease | cyanation | amide resonance | trialkylborane | catalysts | biofilm eradication | pharmacokinetics | N bond activation | pancreatic cancer cells | DMF | aryl esters | Michael acceptor | fumardiamide | water solvation | ester bond activation | cyclization | nuclear magnetic resonance | secondary amides | reaction mechanism | density functional theory | density-functional theory | amino acid transporters
eBook
Advanced synthesis & catalysis, ISSN 1615-4150, 05/2014, Volume 356, Issue 7, pp. 1443 - 1460
(Pentamethylcyclopentadienyl)rhodium (RhCp*)‐catalyzed CH transformations have emerged as a prosperous field in CH bond activation... 
rhodium(III) | Cheteroatom bond formation | CH bond activation | CC bond formation | C-H bond activation | C-C bond formation | C-heteroatom bond formation
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2017, Volume 56, Issue 4, pp. 1073 - 1076
...‐selectively activate the C−H bond located γ to the amino group. Added bulk: A palladium‐catalyzed reaction of primary amines with iodoarenes produces γ... 
amines | reaction mechanisms | palladium | C−H activation | arylation | Palladium | Buttresses | Amines | Hydrogen bonds
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2016, Volume 55, Issue 37, pp. 11000 - 11019
...‐promoted activation of hitherto considered inert C−H bonds is promoting a fundamental change in the field of synthetic chemistry... 
cycloaddition | C−H activation | homogeneous catalysis | heterocycles | transition metals | Catalysis | Chemical bonds
Journal Article
Angewandte Chemie (International ed.), ISSN 1521-3773, 08/2007, Volume 46, Issue 34, pp. 6505 - 6507
Any old iron: Readily available and nontoxic FeCl2 effectively catalyzes CC bond formation by oxidative activation of benzylic C... 
CH activation | iron | cross‐coupling | peroxides | redox chemistry | Iron | Peroxides | Redox chemistry | C-H activation | Cross-coupling
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2019, Volume 58, Issue 1, pp. 307 - 311
...)−H activation under mild conditions enabled by highly variable RhIII‐Cpx catalysts. The method has a wide substrate scope and proceeds with good to excellent yields and enantioselectivities... 
asymmetric catalysis | C−H activation | Hedgehog pathway inhibitors | spiropyrazolones | rhodium | Organic chemistry | Catalysts | Natural products | Chemical reactions | Activation | Enantiomers | Pyrazolones | Substrates | Index Medicus
Journal Article
Synlett, ISSN 0936-5214, 11/2016, Volume 27, Issue 18, pp. 2530 - 2540
...–C bond activation, and briefly discuss other modern developments in this area. 1 Introduction 2 Amide Bond Ground-State Distortion 3 Acyl Amide N–C Cross-Coupling... 
account | Suzuki coupling | decarbonylative coupling | nickel | amides | C-H activation | cross-coupling | palladium | N-C bond activation | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 02/2019, Volume 361, Issue 4, pp. 654 - 672
In the last few decades, the transition metal‐catalyzed activation of inert C−H bonds has led to a fundamental change in the field of synthetic chemistry. Most of these... 
annulation reactions | C−H activation | ruthenium catalysis | heterocycles | Physical Sciences | Chemistry | Chemistry, Organic | Chemistry, Applied | Science & Technology | Ruthenium | Organic chemistry | Transition metals | Hydrogen bonds | Chemical reactions | Activation | Cyclic compounds | Ruthenium compounds | Alkynes
Journal Article