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Chemical Society Reviews, ISSN 0306-0012, 01/2014, Volume 43, Issue 1, pp. 412 - 443
Suzuki-Miyaura (SM) cross-coupling is arguably the most widely-applied transition metal catalysed carbon-carbon bond forming reaction to date. Its success... 
CATALYZED DEHYDROGENATIVE BORYLATION | HETEROCYCLIC CARBENE LIGANDS | ONE-POT SYNTHESIS | ELECTROPHILIC DISPLACEMENT-REACTIONS | TERMINAL ALKYNES | C-H BORYLATION | STEREOSELECTIVE-SYNTHESIS | ASYMMETRIC HYDROBORATION | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | 2-CARBON BUILDING-BLOCK
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 08/2015, Volume 137, Issue 30, pp. 9716 - 9721
The CuH-catalyzed hydroamination of alkenes and alkynes using a silane and an amine transfer reagent represents a simple strategy to access chiral amine... 
ALKENES | O-BENZOYL HYDROXYLAMINES | CONJUGATE REDUCTION | IMINES | 1,3-HALOGEN MIGRATION | ASYMMETRIC ALLYLIC SUBSTITUTION | ELECTROPHILIC AMINATION | ARYL | DIORGANOZINC REAGENTS | C=N BONDS | CHEMISTRY, MULTIDISCIPLINARY | Synthesis | Amines | Design modifications | Reagents | Amino acids | Strategy | Esters | Steroids
Journal Article
CATALYSIS SCIENCE & TECHNOLOGY, ISSN 2044-4753, 3/2019, Volume 9, Issue 5, pp. 173 - 191
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2017, Volume 56, Issue 36, pp. 10938 - 10941
The use of readily available hydroxamic acids as reagents for the chemoselective (ortho‐amino)arylation of amides is described. This reaction proceeds under... 
aminoarylation | chemoselectivity | amides | hydroxamic acids | sigmatropic rearrangement | ELECTROPHILIC ACTIVATION | ALPHA-ARYLATION | C-H OLEFINATION | BOND FORMATION | CARBONYL-COMPOUNDS | TRIFLIC ANHYDRIDE | CATALYTIC HYDROSILYLATION | CHEMISTRY, MULTIDISCIPLINARY | REDUCTION | SECONDARY AMIDES | KETENIMINIUM SALTS | Aniline | Chemical tests and reagents | Amides | Acids | Metals | Reagents | Carbonyls
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2016, Volume 55, Issue 37, pp. 11226 - 11230
Novel methodology for O‐functionalization of carbohydrate derivatives has been established using bench‐stable and easily prepared iodonium(III) reagents. Both... 
carbohydrates | electrophilic addition | hypervalent compounds | arylation | fluorine | GLYCOSIDES | OXIDATION | METAL-FREE ARYLATION | ONE-POT SYNTHESIS | DIARYLIODONIUM SALTS | ARYL ETHERS | GLYCOSYLATION | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | GALECTIN-3 | INHIBITORS | Chemical tests and reagents | Cyclodextrins | Fluorides | Communications | Communication
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 12/2013, Volume 43, Issue 1, pp. 412 - 443
Suzuki-Miyaura (SM) cross-coupling is arguably the most widely-applied transition metal catalysed carbon-carbon bond forming reaction to date. Its success... 
Carbon-carbon composites | Cross coupling | Transition metals | Boron | Chemical reactions | Joining | Samarium | Bonding
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 10/2011, Volume 133, Issue 41, pp. 16410 - 16413
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2015, Volume 54, Issue 38, pp. 11200 - 11204
Journal Article