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Journal of the American Chemical Society, ISSN 0002-7863, 02/2013, Volume 135, Issue 7, pp. 2505 - 2508
A visible-light-mediated hydrotrifluoromethylation of unactivated alkenes that uses the Umemoto reagent as the CF3 source and MeOH as the reductant is... 
MEDICINAL CHEMISTRY | ORGANIC-SYNTHESIS | ACIDS | LIGHT PHOTOREDOX CATALYSIS | BOND FORMATION | FLUORINE | RADICALS | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | TERMINAL ALKENES | TRIFLUOROMETHYLATION | Alkenes - chemistry | Molecular Structure | Catalysis | Methylation | Fluorine - chemistry | Measurement | Thermal properties | Olefins | Analysis | Chemical properties | Activation energy
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 32, pp. 9249 - 9252
A copper‐catalyzed three‐component reaction of alkenes, alkylnitriles, and water affords γ‐butyrolactones in good yields. The domino process involves an... 
multicomponent reactions | copper | total synthesis | alkenes | heterocycles | INTRAMOLECULAR CARBOAMINATION | ALKYL NITRILES | GAMMA-LACTONES | COPPER(I)-CATALYZED REACTION | CHEMISTRY, MULTIDISCIPLINARY | ACTIVATED ALKENES | COOPERATIVE CATALYSIS | ARYL DIAZONIUM SALTS | ALLYLIC ALCOHOLS | METAL-SALTS | TERMINAL ALKENES | Synthesis | Chemical properties | Copper | Olefins | Methods | Organic compounds
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2018, Volume 59, Issue 23, pp. 2302 - 2305
An efficient nickel-catalyzed reductive relay cross-coupling of internal alkenes with alkyl (or aryl) halides has been developed. This method has demonstrated... 
Internal alkenes | Terminal-selectivity | Isomerization | Nickel-catalyzed | Alkylation | HALIDES | ORGANIC-SYNTHESIS | COBALT CATALYSTS | CHEMISTRY, ORGANIC | FORMAL HYDROAMINATION | CROSS-COUPLING REACTIONS | ARYL BORONIC ACIDS | REMOTE FUNCTIONALIZATION | OLEFINS | TERTIARY SILANES | CARBOXYLIC-ACIDS | Olefins
Journal Article
ACS Catalysis, ISSN 2155-5435, 03/2018, Volume 8, Issue 3, pp. 2001 - 2005
The aluminum-catalyzed hydroboration of alkenes with HBpin is reported using simple commercially available aluminum hydride precatalysts [LiAlH4 or sodium... 
main group | catalysis | aluminum | hydroboration | alkene | REDUCTIVE DEHALOGENATION | COMPLEXES | CHEMISTRY, PHYSICAL | CARBONYL-COMPOUNDS | TERMINAL ALKYNES | ALDEHYDES | HYDROALUMINATION | HYDRIDE | SELECTIVE HYDROBORATION | KETONES | BORON REAGENTS
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 05/2017, Volume 139, Issue 20, pp. 6835 - 6838
An intermolecular, three-component reductive dicarbofunctionalization of alkenes is presented here. The combination of Ni catalysis with TDAE as final... 
BORONIC ACIDS | HALIDES | COUPLING REACTIONS | ARYL IODIDES | RADICALS | REDOX-ACTIVE ESTERS | INTERMOLECULAR TRIFLUOROMETHYLARYLATION | ALKYL BROMIDES | ELECTROPHILES | CHEMISTRY, MULTIDISCIPLINARY | TERMINAL ALKENES | Metal catalysts | Olefins | Chemical bonds | Nickel | Chemical properties | Research | Electrophiles
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2017, Volume 56, Issue 19, pp. 5336 - 5340
An asymmetric palladium‐catalyzed intramolecular oxidative aminoarylation of alkenes has been developed with quinoline–oxazoline chiral ligands and Ag 2 CO 3... 
aminoarylation | palladium | asymmetric catalysis | alkenes | heterocycles | OXIDATION | PALLADIUM-CATALYZED CARBOAMINATION | OXAZOLINE LIGANDS | CHEMISTRY, MULTIDISCIPLINARY | UNACTIVATED ALKENES | SOLE OXIDANT | AZA-WACKER REACTIONS | HYDROGEN-PEROXIDE | TERMINAL OLEFINS | CYCLIZATION | MOLECULAR-OXYGEN
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2014, Volume 53, Issue 10, pp. 2730 - 2734
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2015, Volume 54, Issue 3, pp. 801 - 804
The cobalt‐catalyzed selective isomerization of terminal alkenes to the thermodynamically less‐stable (Z)‐2‐alkenes at ambient temperatures takes place by a... 
cobalt | stereoselectivity | alkenes | isomerization | double‐bond migration | Stereoselectivity | Alkenes | Cobalt | Isomerization | Double-bond migration | COMPLEXES | OLEFINS | double-bond migration | CHEMISTRY, MULTIDISCIPLINARY | 1-ALKENES | Thermodynamics | Hydrogen | Olefins | Ambient temperature | Ligands | Formations | Materials selection | Hydrogen atoms | Terminals
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2016, Volume 55, Issue 13, pp. 4308 - 4311
A highly diastereoselective method for the synthesis of dihydroepoxybenzofluorenone derivatives from aromatic/vinylic amides and bicyclic alkenes is described.... 
amides | cobalt | annulation | C−H activation | alkenes | C-H activation | ORGANIC-SYNTHESIS | BOND FUNCTIONALIZATION | SELECTIVE ACCESS | TERMINAL ALKYNES | INTERNAL ALKYNES | TRANSITION-METALS | CHEMISTRY, MULTIDISCIPLINARY | DIRECTING GROUPS | MILD | N-CARBAMOYL INDOLINES | CYCLIZATION | Amides | Cobalt | Olefins | Organic chemistry | Transformation | Cycloaddition | Alkenes | Hydrogen bonds | Chemical reactions | Activation | Functional groups
Journal Article