Keyphrases
Benzyl Fluorides
72%
Amination
48%
Hydrogen Bonds (H-bonds)
45%
DFT Calculations
40%
Transition Structure
39%
Computational Study
39%
C-F Bond
37%
1,3-dipolar Cycloaddition
36%
Acid-catalyzed
36%
Desymmetrization
36%
Chiral Phosphoric Acid
36%
Nucleophile
36%
Aniline
34%
Nucleophilic Substitution
31%
Density Functional Calculations
29%
Friedel-Crafts Reaction
28%
Bioorthogonal
28%
Reaction Mechanism
28%
Elemental Sulfur
27%
Transition State
27%
Polysulfide
27%
Triol
25%
Fluoroarenes
24%
Ring Contraction
24%
Sydnone
24%
Heterohelicene
24%
Hydrogen Donor
24%
Highly Concentrated
24%
Oxetane
24%
Iminosydnone
24%
Sulfonamides
24%
Substituent Effect
24%
Stereocontrolled
24%
Cycloaddition
24%
M06-2X
23%
Nucleophilic
21%
Dipole
20%
Regioselectivity
20%
Chemical Biology
20%
Mesoionic
20%
Reaction Conditions
20%
Functional Groups
19%
Density Functional Theory
18%
Stereospecific
18%
Friedel-Crafts Acylation
18%
Diaryl
18%
Arynes
18%
Stereochemical Hypothesis
18%
Nucleophilic Radiofluorination
16%
Cross-coupling
16%
Chemistry
Density Functional Theory
100%
Hydrogen Bonding
68%
Nucleophile
47%
1,3-cycloaddition
36%
Phosphoric Acid
36%
Nucleophilic Substitution
34%
Friedel-Crafts Reaction
30%
Alkene
30%
Cation
30%
Triol
30%
Elemental Sulfur
28%
Hydrogen
28%
Transition State
26%
Enantioselectivity
25%
Fluoroarene
24%
Ring Contraction
24%
Aryne
24%
Carbocation
24%
Oxetane
24%
Sulfonamide
24%
Donor
22%
Lewis Acid
18%
Alkyne
18%
Benzylation
18%
Chemistry
16%
Regioselectivity
16%
Helicene
16%
Pyrazole
15%
Substituent Effect
15%
Elimination Reaction
15%
Isocyanate
14%
Thiourea
14%
Electrophile
13%
Fluorination
12%
Cycloalkyne
12%
Imine
12%
Azomethine Ylide
12%
Chalcone
12%
Azetidine
12%
Enone
12%
Trifluoroacetic Acid
12%
Benzyl Alcohol
12%
Diarylmethane
12%
Triarylmethane
12%
Oxacycle
12%
Ambient Reaction Temperature
12%
Aminoquinoline
12%
Fischer Synthesis
12%
Grignard Reagent
12%
Selenide
12%