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01/2019, ISBN 3039212044
The amide bond represents a privileged motif in chemistry. The recent years have witnessed an explosion of interest in the development of new chemical... 
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 | cyclopentadienyl complexes | C-S formation | enzymes | DFT study | sulfonamide bond | 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
Chemistry – A European Journal, ISSN 0947-6539, 03/2017, Volume 23, Issue 14, pp. 3496 - 3496
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2016, Volume 55, Issue 24, pp. 6959 - 6963
The first Ni‐catalyzed Suzuki–Miyaura coupling of amides for the synthesis of widely occurring biaryl compounds through N−C amide bond activation is reported.... 
cross-coupling | N−C activation | nickel | amide bonds | biaryls | N-C activation | PALLADIUM | C CLEAVAGE | ACTIVATION | CARBOXYLATES | TWISTED AMIDES | CHEMISTRY, MULTIDISCIPLINARY | ETHERS | CROSS-COUPLINGS | RESONANCE | N ROTATIONAL PATHWAY | LACTAMS | Amides | Nickel
Journal Article
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2011, Volume 50, Issue 47, pp. 11197 - 11201
Give me an N: The catalytic amination of α‐hydroxy amides with a variety of amines, including anilines, primary and secondary aliphatic amines, and ammonia,... 
amines | ruthenium | homogeneous catalysis | α‐hydroxy amides | α‐amino acid amides | α-hydroxy amides | α-amino acid amides | Amines - chemistry | Amination | Amides - chemical synthesis | Amides - chemistry | Amino Acids - chemistry | Esters | Molecular Structure | Ammonia - chemistry | Aniline Compounds - chemistry | Catalysis | Ruthenium - chemistry
Journal Article
Organic & Biomolecular Chemistry, ISSN 1477-0520, 01/2018, Volume 16, Issue 43, pp. 7998 - 8010
Cross-coupling reactions are among the most powerful C–C and C–X bond forming tools in organic chemistry. Traditionally, cross-coupling methods rely on the use... 
Cross coupling | Amides | Chemical reactions | Activation | Carbon | Couplings | Organic chemistry | Halides | Aromatic compounds | Construction methods | Extrusion | Functional groups | Coupling methods
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 09/2019, Volume 2019, Issue 33, p. 5812
Metal-free and Selectfluor-mediated C-S bond cleavage is described. This novel strategy provides a facile and efficient method to access important... 
Amides
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 11/2018, Volume 16, Issue 43, pp. 7998 - 81
Cross-coupling reactions are among the most powerful C-C and C-X bond forming tools in organic chemistry. Traditionally, cross-coupling methods rely on the use... 
ACYCLIC AMIDES | ELECTRONICALLY-ACTIVATED AMIDES | SECONDARY AMIDES | N-C CLEAVAGE | CATALYZED CARBONYLATION REACTIONS | TWISTED AMIDES | CHEMISTRY, ORGANIC | BOND FORMATION | CHEMOSELECTIVE KETONE SYNTHESIS | ACYL-TRANSFER REAGENTS | GENERAL-METHOD
Journal Article