Keyphrases
Acetic Acid Derivative
50%
Activation Barrier
16%
Alcohol-assisted
16%
Alder-Rickert Reaction
25%
Alkylthio
16%
Allyl Methacrylate
25%
Benzofuranone
50%
Benzofuranone Derivative
50%
Benzylidene
16%
Catalytic Motif
16%
Chelates
16%
Chromanone Derivatives
50%
Claisen
50%
Counterion
50%
Cyclization
50%
Derivative Synthesis
50%
DFT Calculations
16%
Diels-Alder Cycloaddition
25%
Hydride Transfer
16%
Imidazole
50%
Imidazolone
50%
Keys to Success
16%
Kopsia Alkaloids
50%
Malonate
16%
Mannich
25%
Meso
17%
Metal-organic Frameworks (MOFs)
50%
Mukaiyama Aldol
25%
NMR Analysis
16%
Nucleophilic Ring-opening Reactions
50%
Palladium
17%
Percentage Yield
16%
Porphyrin-phospholipid
100%
Porphyrinates
20%
Proton Conductivity
100%
Silylation
25%
Structural Transformation
57%
Styrene
16%
Substituted Benzaldehydes
50%
Sulfur
16%
Sulfur Derivatives
16%
Tetrahydro-β-carboline
25%
Tetrakis
17%
Theoretical Comparison
16%
Thioether
50%
Thiol Chemistry
16%
Transitional Geometry
16%
Tsuji-Trost
50%
Tsuji-Trost Allylation
50%
Ytterbium Trifluoride
50%
Chemistry
Acetic Acid
50%
Alder-Rickert Cycloaddition
16%
Ammonia
14%
Benzaldehyde
25%
Boron Trifluoride
50%
Chemistry
14%
Chromanone
25%
Claisen Rearrangement
50%
Claisen-Ireland Rearrangement
25%
Claisen-Johnson Rearrangement
50%
Counterion
50%
Crystal Structure
17%
Crystallinity
7%
Cyclopropane
50%
Cystamine
7%
Diastereomer
16%
Dimethyl Sulfoxide
25%
Donor
16%
Eschenmoser-Claisen Rearrangement
25%
formation
15%
Heterocyclic Compound
16%
Hydrogen Bonding
7%
Hydrogen-Bonded Organic Framework
100%
hydrolytic
10%
Imidazole
50%
Ionic Conductivity
8%
Kopsinine
16%
Macrocycle
17%
Mechanistic Study
25%
Metal Organic Framework
100%
Palladium
35%
Photocatalyst
25%
Photochemical Reaction
50%
Photocyclization
25%
Porphyrin
32%
Powder Diffraction
10%
Proton Conductor
17%
Ring Opening Reaction
50%
Thermal Stability
10%
Thiocyanate
7%
Thiol
50%
Triflate
50%
Tsuji-Trost Allylation
50%
Ytterbium
50%
