Keyphrases
Arynes
100%
Alkyl
87%
Regioselectivity
64%
Carbodicarbene
54%
Redox-active Ligands
54%
1,3-dienes
50%
Percentage Yield
47%
Tris
41%
Metal-catalyzed
36%
Nucleophile
36%
Hydroarylation
33%
Triflate
33%
Dienes
33%
Rhodium Catalysis
33%
Rh-catalyzed
33%
Five-membered
33%
Early Transition Metal
31%
Difunctionalization
31%
Allyl
30%
Cross-coupling
29%
Alkyl Complexes
25%
Rh(III)
25%
Amido
23%
Tridentate
22%
Redox-active
22%
Bisphosphine
22%
Rhodium Complexes
20%
Structural Properties
20%
Enantioselectivity
20%
Ligand-controlled
20%
Ketimines
20%
Palladium Catalysis
20%
Annulation
20%
Metal-free
19%
Rh Complex
19%
Site-selective
18%
Ketoiminate
16%
Lutetium
16%
Phosphinooxazolines
16%
Mechanistic Understanding
16%
Redox Catalysis
16%
Lewis Acid Activation
16%
Cross-coupling Catalysis
16%
Reactor Kinetics
16%
Nickel(III)
16%
C-H Cleavage
16%
Two-electron Redox
16%
Polymer-supported Catalyst
16%
Redox
16%
Tetrakis
16%
Chemistry
Aryne
93%
Tris
72%
Donor
61%
Regioselectivity
60%
Rhodium
50%
Transition Metal
50%
Nucleophile
45%
Hydroarylation
33%
Triflate
33%
formation
30%
EPR Spectroscopy
29%
UV/VIS Spectroscopy
25%
Carboxylic Acid
22%
Heterocyclic Compound
20%
NMR Spectroscopy
20%
Imine
20%
Ring Formation
19%
Palladium
19%
electronics
19%
Redox Catalysis
16%
Lutetium
16%
Ring Opening Polymerisation
16%
Polymerization Catalyst
16%
Ambient Reaction Temperature
16%
Hydroamination
16%
Lewis Acid
16%
Butenolide
16%
Umpolung
16%
Vinylarene
16%
Trifluoromethylation
16%
Heteroarene
16%
Oxidative Addition
16%
Crystal Structure
16%
Hydrogen
16%
Transition Metal Catalysis
16%
Halide
16%
Base
16%
Allene
16%
Catalyst Activation
16%
Electrophile
16%
Indole
16%
Lithium Salt
16%
Magnesium
16%
Density Functional Theory
16%
Carboxamide
16%
Boronate Ester
16%
Pincer Complex
16%
Coordination Sphere
16%
Organometallic Chemistry
16%
Triple Bond
16%
