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Journal of the American Chemical Society, ISSN 0002-7863, 1900, Volume 137, Issue 31, pp. 9843 - 9854
The origin of the high reactivity and site selectivity of pyridine N-oxide substrates in O-pivaloyl hydroxamic acid-directed Rh­(III)-catalyzed (4+2... 
Oxidation-Reduction | Pyridines - chemistry | Molecular Conformation | Models, Molecular | Alkynes - chemistry | Catalysis | Kinetics | Binding Sites | Hydrogen - chemistry | Carbon - chemistry | Rhodium - chemistry | Index Medicus
Journal Article
Organic letters, ISSN 1523-7060, 07/2014, Volume 16, Issue 13, pp. 3556 - 3559
Secondary amines react with thiosalicylaldehydes in the presence of catalytic amounts of acetic acid to generate ring-fused N,S-acetals in redox-neutral fashion... 
Amines - chemistry | Protons | Oxidation-Reduction | Acetals - chemical synthesis | Acetic Acid - chemistry | Molecular Structure | Piperazines - chemistry | Catalysis | Acetals - chemistry | Morpholines - chemistry | Index Medicus | Letter
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 01/2014, Volume 136, Issue 3, pp. 894 - 897
A combined experimental/computational study on the amino acid ligand-assisted Pd-catalyzed C–H bond activation reveals a mechanism in which the amino acid acts... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Protons | Hydrocarbons, Aromatic - chemistry | Stereoisomerism | Molecular Conformation | Amino Acids - chemistry | Models, Molecular | Substrate Specificity | Ligands | Catalysis | Palladium - chemistry | Carbon - chemistry | Computational chemistry | Amino acids | Usage | Analysis | Index Medicus
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 03/2012, Volume 51, Issue 10, pp. 2391 - 2394
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 02/2007, Volume 129, Issue 6, pp. 1805 - 1815
.... The latter require rather small reorganization energies for electron transfer (<0.20 eV) making these compounds promising candidates for n-channel... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 06/2016, Volume 138, Issue 21, pp. 6861 - 6868
.... We report density functional theory (B3LYP and M06) investigations on the mechanism of rhodium­(III)-catalyzed redox coupling reaction of N-phenoxyacetamides with alkynes... 
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 10/2014, Volume 136, Issue 39, pp. 13769 - 13780
.... The acidity of the Brønsted acid is crucial for the catalytic efficiency: the less acidic phosphoric acids are ineffective, while highly acidic chiral N-triflylphosphoramides are very efficient and can promote highly enantioselective cycloadditions... 
Density functionals | Chemical properties | Phosphors | Analysis | Olefins
Journal Article
Journal of the American Chemical Society, ISSN 1520-5126, 05/2016, Volume 138, Issue 21, pp. 6861 - 6868
...(III)-catalyzed redox coupling reaction of N-phenoxyacetamides with alkynes. The results elucidated the role of the internal oxidizing directing group, and the role of Rh-III/Rh-I and Rh-III/Rh-V catalysis of C-H functionalizations... 
Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology
Journal Article
Accounts of chemical research, ISSN 0001-4842, 04/2013, Volume 46, Issue 4, pp. 979 - 989
This Account describes how attractive interactions of aromatic rings with other groups can influence and control the stereoselectivity of many reactions.... 
Benzyl Alcohols - chemistry | Cyclization | Furans - chemistry | Stereoisomerism | Binding Sites | Oxazolidinones - chemistry | Research | Chemical properties | Stereochemistry | Aromatic compounds | Nuclear reactions | Quantum theory | Index Medicus | Stereoselectivity | Asymmetry | Accessibility | Quantum mechanics | Chemical reactions | Mathematical models | Hydrogenation
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 08/2017, Volume 56, Issue 34, pp. 10070 - 10086
The activation strain or distortion/interaction model is a tool to analyze activation barriers that determine reaction rates. For bimolecular reactions, the... 
chemical reactivity | quantum chemistry | reaction mechanisms | transition states | computational chemistry | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Activation energy | Analysis | Distortion | Activation analysis | Reviews | Review
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 03/2014, Volume 20, Issue 12, pp. 3365 - 3375
Journal Article