Keyphrases
Calixarene
100%
Reductive Elimination
56%
Aryl
47%
Arenes
46%
Calix
37%
Tert
24%
Room Temperature
23%
Difluoro
23%
Inclusion Complex
22%
Pt(II) Complexes
20%
Electrophilic Fluorination
19%
Rhodium
18%
Methyl
18%
Oxidative Addition
18%
Pt(IV) Complexes
17%
Methylene
17%
Bond Activation
17%
XeF2
16%
Platinum(II)
16%
Rhodium Complexes
16%
C-H Activation
15%
Metal-ligand Cooperation
15%
Fluorophore
15%
Aromatization
15%
Pt(IV)
15%
Elimination Reactions
15%
Pincer Complexes
14%
Bimetallic
14%
C-C Activation
13%
Metal-mediated
12%
Phosphine Complexes
12%
Phosphine Ligands
12%
Acetone
12%
Oxygen Atom
12%
Palladium(II)
12%
Catalytic Applications
12%
Quinone Methide
12%
C-H Bond Activation
11%
Aryl Iodides
11%
Carbon-halogen Bond
11%
Aryl Fluorides
11%
Aromatic Ring
11%
Aryl Groups
11%
Chelates
11%
Zinc
10%
Nucleophilic Substitution
10%
Hydrogen Bonds (H-bonds)
10%
Agostic
10%
Organic Synthesis
10%
Neat Conditions
10%
Chemistry
Calixarene
96%
Reductive Elimination Reaction
58%
Rhodium
41%
Chemistry
37%
Calix[4]arene
35%
Complexation
31%
Ambient Reaction Temperature
26%
Palladium
24%
Density Functional Theory
22%
Oxidative Addition
22%
Electrophilic Fluorination
21%
Alkene
21%
Halide
20%
Quinone
18%
Pincer Complex
17%
Metallocene
17%
C-H Bond Activation
15%
Transition Element
14%
Fluorine
13%
Oxygen Atom
12%
Aryl Group
12%
Nucleophilic Substitution
12%
Aromatic Structure
12%
Cation
12%
Multicomponent Reaction
10%
Methanol
10%
Pyrazole
9%
Electron Density
9%
Trimethylbenzene
9%
Cross-Coupling Reaction
9%
Sodium
9%
Dinitrogen
9%
Fluorination
8%
Double Bond
8%
NMR Spectroscopy
8%
Donor
7%
Iodoarene
7%
Purity
7%
Passerini Condensation
7%
19F NMR Spectroscopy
7%
Metal Ion
7%
Coordination Compound
7%
Polypeptide
7%
Carbazole
7%
Arylation
7%
Base
7%
Ethylene
7%
Dichloromethane
7%
Calixarene Complex
6%
13C NMR Spectroscopy
6%