Angewandte Chemie International Edition, ISSN 1433-7851, 09/2014, Volume 53, Issue 38, pp. 10090 - 10094
Carbonylation reactions represent useful tools for organic synthesis. However, the necessity to use gaseous carbon monoxide is a disadvantage for most organic...
reaction mechanisms | palladium | arenes | carbonylation | synthetic methods | VINYLIC HALIDES | ALKOXYCARBONYLATION | REDUCTIVE CARBONYLATION | CHEMISTRY, MULTIDISCIPLINARY | N-FORMYLSACCHARIN | FORMYLATION | SITU GENERATION | STOICHIOMETRIC CARBON-MONOXIDE | MICROWAVE-ENHANCED AMINOCARBONYLATIONS | EFFICIENT | CO SOURCE | Arenes | Carbonylation | Palladium | Synthetic methods | Reaction mechanisms | Aldehydes | Esters | Conduction | Synthesis | Aromatic compounds | Chemists | Bromides | Carbon monoxide | Carbonyls
reaction mechanisms | palladium | arenes | carbonylation | synthetic methods | VINYLIC HALIDES | ALKOXYCARBONYLATION | REDUCTIVE CARBONYLATION | CHEMISTRY, MULTIDISCIPLINARY | N-FORMYLSACCHARIN | FORMYLATION | SITU GENERATION | STOICHIOMETRIC CARBON-MONOXIDE | MICROWAVE-ENHANCED AMINOCARBONYLATIONS | EFFICIENT | CO SOURCE | Arenes | Carbonylation | Palladium | Synthetic methods | Reaction mechanisms | Aldehydes | Esters | Conduction | Synthesis | Aromatic compounds | Chemists | Bromides | Carbon monoxide | Carbonyls
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2017, Volume 56, Issue 23, pp. 6384 - 6394
Methanol is used as a common solvent, cost‐effective reagent, and sustainable feedstock for value‐added chemicals, pharmaceuticals, and materials. Among the...
methanol | esterification | formylation | methylation | methoxylation | Methylation | Methanol
methanol | esterification | formylation | methylation | methoxylation | Methylation | Methanol
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2016, Volume 358, Issue 3, pp. 336 - 352
Dimethyl sulfoxide (DMSO) is one of the most commonly applied organic solvents in chemical transformations and is utilized widely in industrial processes as...
dimethyl sulfoxide (DMSO) | oxidation | organic synthesis | synthetic methodology | C1 source | one‐carbon source | one-carbon source | source | C-1 source | ONE-POT SYNTHESIS | DOMINO OXIDATIVE CYCLIZATION | CHEMISTRY, ORGANIC | BOND FORMATION | ALPHA-KETOAMIDES | C-H FUNCTIONALIZATION | METAL-FREE APPROACH | N-METHYLATION | CROSS-COUPLING REACTIONS | CHEMISTRY, APPLIED | ARYL METHYL KETONES | 6-PI-2-AZATRIENE ELECTROCYCLIZATION | Chemical tests and reagents | Production processes | Dimethyl sulfoxide | Solvents | Synthesis | Oxidants | Employment | Reagents | Transformations | Catalysis
dimethyl sulfoxide (DMSO) | oxidation | organic synthesis | synthetic methodology | C1 source | one‐carbon source | one-carbon source | source | C-1 source | ONE-POT SYNTHESIS | DOMINO OXIDATIVE CYCLIZATION | CHEMISTRY, ORGANIC | BOND FORMATION | ALPHA-KETOAMIDES | C-H FUNCTIONALIZATION | METAL-FREE APPROACH | N-METHYLATION | CROSS-COUPLING REACTIONS | CHEMISTRY, APPLIED | ARYL METHYL KETONES | 6-PI-2-AZATRIENE ELECTROCYCLIZATION | Chemical tests and reagents | Production processes | Dimethyl sulfoxide | Solvents | Synthesis | Oxidants | Employment | Reagents | Transformations | Catalysis
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1344 - 9
N-Methylated amines play an important role in regulating the biological and pharmaceutical properties of all kinds of life science molecules. In general, this...
MILD | FORMIC-ACID | METHYLATION | EPIGENETICS | PEPTIDES | NITRO-COMPOUNDS | AMINES | MULTIDISCIPLINARY SCIENCES | COMPLEXES | CARBON-DIOXIDE | EFFICIENT | Biological properties | Drugs | Amitriptyline | Amines | Iodides | Iron | High pressure | Hydrogen reduction | Dimethyl sulfate | Imipramine | Amination | Venlafaxine | Methyl compounds | Life sciences | Sulfate | Drug discovery | Iron oxides | Methylation | Chemical synthesis | Hydrogen ion concentration
MILD | FORMIC-ACID | METHYLATION | EPIGENETICS | PEPTIDES | NITRO-COMPOUNDS | AMINES | MULTIDISCIPLINARY SCIENCES | COMPLEXES | CARBON-DIOXIDE | EFFICIENT | Biological properties | Drugs | Amitriptyline | Amines | Iodides | Iron | High pressure | Hydrogen reduction | Dimethyl sulfate | Imipramine | Amination | Venlafaxine | Methyl compounds | Life sciences | Sulfate | Drug discovery | Iron oxides | Methylation | Chemical synthesis | Hydrogen ion concentration
Journal Article
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Full Text
Transition-Metal-Catalyzed Utilization of Methanol as a C-1 Source in Organic Synthesis
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, ISSN 1433-7851, 06/2017, Volume 56, Issue 23, pp. 6384 - 6394
Methanol is used as a common solvent, cost-effective reagent, and sustainable feedstock for value-added chemicals, pharmaceuticals, and materials. Among the...
SELECTIVE OXIDATION | formylation | CARBONYLATION REACTIONS | N-FORMYLATION | CHEMISTRY, MULTIDISCIPLINARY | PRIMARY ALCOHOLS | ARYL BROMIDES | esterification | AMINES | methylation | methoxylation | GREEN CHEMISTRY | methanol | AEROBIC OXIDATION | EFFICIENT
SELECTIVE OXIDATION | formylation | CARBONYLATION REACTIONS | N-FORMYLATION | CHEMISTRY, MULTIDISCIPLINARY | PRIMARY ALCOHOLS | ARYL BROMIDES | esterification | AMINES | methylation | methoxylation | GREEN CHEMISTRY | methanol | AEROBIC OXIDATION | EFFICIENT
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 07/2014, Volume 53, Issue 29, pp. 7579 - 7583
A new approach for the facile synthesis of fused quinazolinone scaffolds through a palladium‐catalyzed carbonylative coupling followed by an intramolecular...
nucleophilic aromatic substitution | palladium catalysts | domino reactions | carbonylation | quinazolinones | ULLMANN CONDENSATION | PYRIDOQUINAZOLONES | ONE-POT SYNTHESIS | 4(3H)-QUINAZOLINONES | CHEMISTRY, MULTIDISCIPLINARY | NUCLEOPHILES | CYCLOADDITION | HETEROCYCLES | RUTAECARPINE | DERIVATIVES | Models, Molecular | Crystallography, X-Ray | Quinazolinones - chemistry | Catalysis | Isomerism | Palladium - chemistry | Palladium catalysts | Substitution reactions | Palladium | Diels-Alder reactions | Quinazolinones | Synthesis | Joining | Formations | Derivatives | Isomers | Modulators | Carbonyls
nucleophilic aromatic substitution | palladium catalysts | domino reactions | carbonylation | quinazolinones | ULLMANN CONDENSATION | PYRIDOQUINAZOLONES | ONE-POT SYNTHESIS | 4(3H)-QUINAZOLINONES | CHEMISTRY, MULTIDISCIPLINARY | NUCLEOPHILES | CYCLOADDITION | HETEROCYCLES | RUTAECARPINE | DERIVATIVES | Models, Molecular | Crystallography, X-Ray | Quinazolinones - chemistry | Catalysis | Isomerism | Palladium - chemistry | Palladium catalysts | Substitution reactions | Palladium | Diels-Alder reactions | Quinazolinones | Synthesis | Joining | Formations | Derivatives | Isomers | Modulators | Carbonyls
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2016, Volume 55, Issue 8, pp. 2782 - 2786
The CF3 group is an omnipresent motif found in many pharmaceuticals, agrochemicals, catalysts, materials, and industrial chemicals. Despite well‐established...
palladium | C−H activation | arenes | radical chemistry | fluorine | C-H activation | ROOM-TEMPERATURE | SILVER-MEDIATED TRIFLUOROMETHYLATION | SANDMEYER TRIFLUOROMETHYLATION | OXIDATIVE TRIFLUOROMETHYLATION | HETEROAROMATIC-COMPOUNDS | AROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | PHOTOREDOX CATALYSIS | PD(II)-CATALYZED ORTHO-TRIFLUOROMETHYLATION | C-H TRIFLUOROMETHYLATION | BOND-FORMATION | Pentoxifylline | Palladium | Fluorides | Theophylline | Caffeine | Agricultural chemicals | Melatonin | Catalysts | Materials selection | Chemicals | Organic chemistry | Agrochemicals | Aromatic compounds | Chemical synthesis | Pharmaceuticals
palladium | C−H activation | arenes | radical chemistry | fluorine | C-H activation | ROOM-TEMPERATURE | SILVER-MEDIATED TRIFLUOROMETHYLATION | SANDMEYER TRIFLUOROMETHYLATION | OXIDATIVE TRIFLUOROMETHYLATION | HETEROAROMATIC-COMPOUNDS | AROMATIC-COMPOUNDS | CHEMISTRY, MULTIDISCIPLINARY | PHOTOREDOX CATALYSIS | PD(II)-CATALYZED ORTHO-TRIFLUOROMETHYLATION | C-H TRIFLUOROMETHYLATION | BOND-FORMATION | Pentoxifylline | Palladium | Fluorides | Theophylline | Caffeine | Agricultural chemicals | Melatonin | Catalysts | Materials selection | Chemicals | Organic chemistry | Agrochemicals | Aromatic compounds | Chemical synthesis | Pharmaceuticals
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 11/2015, Volume 21, Issue 46, pp. 16370 - 16373
A novel palladium‐catalyzed CO‐gas‐ and autoclave‐free protocol for the synthesis of 11H‐pyrido[2,1‐b]quinazolin‐11‐ones has been developed. Quinazolinones,...
CH activation | palladium | DMF | heterocycles | carbonylation | C-H activation | Quinazolinones | Isotope effect | Synthesis | Activation | Tolerances | Autoclaving | Bonding | Carbonyls
CH activation | palladium | DMF | heterocycles | carbonylation | C-H activation | Quinazolinones | Isotope effect | Synthesis | Activation | Tolerances | Autoclaving | Bonding | Carbonyls
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 12/2014, Volume 20, Issue 49, pp. 16107 - 16110
A systematic study on the carbonylative transformation of 1‐bromo‐2‐fluorobenzenes with various nucleophiles has been performed. Different types of double...
palladium | domino reactions | heterocycles | nucleophilic substitution | carbonylation | Heterocycles | Domino reactions | Carbonylation | Palladium | Nucleophilic substitution | OXIDATIVE CARBONYLATION | HALIDES | ORGANIC-SYNTHESIS | CROSS-COUPLING REACTIONS | METAL | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | Cytokinins | Quinazolinones | Joining | Transformations | Nucleophiles | Carbonyls
palladium | domino reactions | heterocycles | nucleophilic substitution | carbonylation | Heterocycles | Domino reactions | Carbonylation | Palladium | Nucleophilic substitution | OXIDATIVE CARBONYLATION | HALIDES | ORGANIC-SYNTHESIS | CROSS-COUPLING REACTIONS | METAL | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | Cytokinins | Quinazolinones | Joining | Transformations | Nucleophiles | Carbonyls
Journal Article
ACS Catalysis, ISSN 2155-5435, 03/2015, Volume 5, Issue 3, pp. 1526 - 1529
Nanoscaled iron oxides on carbon were modified with nitrogen-doped graphene (NGr) and found to be excellent catalysts for the chemoselective transfer...
formic acid | iron nanocatalysis | transfer hydrogenation | nitroarenes | anilines | OXIDATION | ASYMMETRIC TRANSFER HYDROGENATION | LOWER OLEFINS | COMPLEXES | CHEMISTRY, PHYSICAL | ALCOHOLS | REDUCTION | NITRILES | AMINES | CATALYSTS | WATER
formic acid | iron nanocatalysis | transfer hydrogenation | nitroarenes | anilines | OXIDATION | ASYMMETRIC TRANSFER HYDROGENATION | LOWER OLEFINS | COMPLEXES | CHEMISTRY, PHYSICAL | ALCOHOLS | REDUCTION | NITRILES | AMINES | CATALYSTS | WATER
Journal Article
Angewandte Chemie, ISSN 1433-7851, 06/2017, Volume 56, Issue 23, p. 6384
Methanol is used as a common solvent, cost-effective reagent, and sustainable feedstock for value-added chemicals, pharmaceuticals, and materials. Among the...
Drugs | Reviews | Natural products | Reagents | Chemical bonds | Methylation | Chemical synthesis | Carbon | Chemicals | Methanol
Drugs | Reviews | Natural products | Reagents | Chemical bonds | Methylation | Chemical synthesis | Carbon | Chemicals | Methanol
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 11/2019
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 11/2015, Volume 56, Issue 46, pp. 6413 - 6416
An interesting Pd/C-catalyzed carbonylative cyclization of -arylpyridin-2-amine derivatives via C–H activation has been developed. With DMF as the CO source,...
CO surrogates | Heterocycle synthesis | Heterogeneous catalyst | C–H activation | Carbonylation | C-H activation | HALIDES | PALLADIUM | SUBSTITUTION | MONOXIDE-FREE AMINOCARBONYLATION | AMIDE SOURCE | OXIDATIVE AMINOCARBONYLATION | CHEMISTRY, ORGANIC | ARYL BROMIDES | CARBON-MONOXIDE | CONSTRUCTION | BOND ACTIVATION | Dimethylformamide
CO surrogates | Heterocycle synthesis | Heterogeneous catalyst | C–H activation | Carbonylation | C-H activation | HALIDES | PALLADIUM | SUBSTITUTION | MONOXIDE-FREE AMINOCARBONYLATION | AMIDE SOURCE | OXIDATIVE AMINOCARBONYLATION | CHEMISTRY, ORGANIC | ARYL BROMIDES | CARBON-MONOXIDE | CONSTRUCTION | BOND ACTIVATION | Dimethylformamide
Journal Article
CHEMISTRY-A EUROPEAN JOURNAL, ISSN 0947-6539, 11/2015, Volume 21, Issue 46, pp. 16370 - 16373
A novel palladium-catalyzed CO-gas- and autoclave-free protocol for the synthesis of 11H-pyrido[2,1-b]quinazolin-11-ones has been developed. Quinazolinones,...
OXIDATIVE CARBONYLATION | C(SP)-H BONDS | MONOXIDE-FREE AMINOCARBONYLATION | FORMAMIDES | CHEMISTRY, MULTIDISCIPLINARY | H ACTIVATION | CROSS-COUPLING REACTIONS | CH activation | DIRECT AMINATION | heterocycles | ARYL HALIDES | CONSTRUCTION | palladium | DMF | carbonylation
OXIDATIVE CARBONYLATION | C(SP)-H BONDS | MONOXIDE-FREE AMINOCARBONYLATION | FORMAMIDES | CHEMISTRY, MULTIDISCIPLINARY | H ACTIVATION | CROSS-COUPLING REACTIONS | CH activation | DIRECT AMINATION | heterocycles | ARYL HALIDES | CONSTRUCTION | palladium | DMF | carbonylation
Journal Article
Catalysis Science and Technology, ISSN 2044-4753, 07/2015, Volume 5, Issue 9, pp. 4474 - 4480
Quinazolinones are of interest in the fields of pharmaceuticals and medicinal chemistry. The application of palladium on activated charcoal (Pd/C) as a...
QUINAZOLINONES | CHARCOAL | PALLADIUM | COUPLING REACTIONS | ACIDS | CHEMISTRY, PHYSICAL | SUZUKI-MIYAURA REACTIONS | PD/C | SALTS | Quinazolinones | Synthesis | Amines | Catalysts | Ligands | Palladium | Phosphines | Carbonyls
QUINAZOLINONES | CHARCOAL | PALLADIUM | COUPLING REACTIONS | ACIDS | CHEMISTRY, PHYSICAL | SUZUKI-MIYAURA REACTIONS | PD/C | SALTS | Quinazolinones | Synthesis | Amines | Catalysts | Ligands | Palladium | Phosphines | Carbonyls
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 12/2015, Volume 21, Issue 49, pp. 17541 - 17541
Journal Article
Catalysis Science & Technology, ISSN 2044-4753, 2015, Volume 5, Issue 9, pp. 4474 - 4480
Quinazolinones are of interest in the fields of pharmaceuticals and medicinal chemistry. The application of palladium on activated charcoal (Pd/C) as a...
Journal Article
Journal of Nanoparticle Research, ISSN 1388-0764, 4/2011, Volume 13, Issue 4, pp. 1593 - 1604
The size, surface charge and agglomeration state of nanoparticles under physiological conditions are fundamental parameters to be determined prior to their...
Nanoparticles | BSA | Toxicology | Optics, Optoelectronics, Plasmonics and Optical Devices | Physical Chemistry | Characterization and Evaluation of Materials | Material Science | Agglomeration | Inorganic Chemistry | Characterisation | Silica | Nanotechnology | OXIDE | SUSPENSIONS | SPHERES | MATERIALS SCIENCE, MULTIDISCIPLINARY
Nanoparticles | BSA | Toxicology | Optics, Optoelectronics, Plasmonics and Optical Devices | Physical Chemistry | Characterization and Evaluation of Materials | Material Science | Agglomeration | Inorganic Chemistry | Characterisation | Silica | Nanotechnology | OXIDE | SUSPENSIONS | SPHERES | MATERIALS SCIENCE, MULTIDISCIPLINARY