Chemical Compounds
Arylation
100%
Aromatic Ester
72%
Total Synthesis
51%
Biaryl
47%
Catalyst
44%
Occurrence in Nature
38%
Coupling Reaction
38%
Palladium
33%
Ester
31%
Heteroarene
29%
Haloarene
29%
Azole
28%
Thiophene
27%
Arene
25%
Nitroarene
24%
Bromoarene
24%
Ligand
24%
Thiophenes
23%
Chemical Transformation
21%
Electrophile
20%
Enantioselectivity
19%
Iodoarene
18%
Pharmaceutical
18%
Molecule
18%
Diazo Compound
17%
Aryl Group
17%
Suzuki-Miyaura Coupling
16%
Phenol
15%
Alkenylation
15%
Thiazoles
15%
Cycloaddition
15%
Aldol Reaction
14%
Chemistry
14%
Regioselectivity
14%
Benzoxazole
14%
Cross-Coupling Reaction
13%
Nucleophile
13%
Proline
13%
Fumagillin
13%
Allylation
13%
Pivalate
13%
Amine
12%
Chemoselectivity
12%
Fluorination
12%
Structure-Activity Relationship
11%
Alkaloid
11%
Ynamide
11%
Acid
10%
Medicine & Life Sciences
Palladium
47%
Catalysis
45%
Esters
42%
Nickel
35%
Thiophenes
31%
Alkenes
23%
Azoles
21%
Arabidopsis
21%
Circadian Clocks
19%
Ligands
19%
Thiazoles
18%
Benzoxazoles
15%
Biological Products
15%
Rhodium
15%
Cycloaddition Reaction
14%
3-hydroxybutanal
13%
Structure-Activity Relationship
13%
Ketones
12%
Casein Kinase I
11%
Organophosphorus Compounds
11%
Amines
11%
TAK 779
10%
Density Functional Theory
10%
Halogenation
10%
Cyclization
9%
PHA 767491
9%
2,2'-Dipyridyl
9%
muscoride A
9%
panepophenanthrin
9%
palladium chloride
9%
Metals
9%
azaspirene
9%
palau'amine
9%
massadine
8%
Phenol
8%
epolactaene
8%
Zirconocene dichloride
8%
Pyrroles
8%
Cyclopropanes
8%
dimethyldioxirane
8%
Lactams
8%
pseurotin
8%
Proline
8%
cyclopropylamine
7%
cyanohydrin
7%
Acids
7%
Alcohols
7%
Lewis Acids
7%
Gadiformes
7%
Bromides
7%
Engineering & Materials Science
Esters
33%
Thiophene
33%
Alkaloids
28%
Catalysis
26%
Nickel
25%
Catalysts
23%
Cyclization
23%
Drug products
17%
Phenols
17%
Derivatives
17%
Ketones
16%
Palladium
15%
Acids
15%
Ligands
14%
Molecules
14%
Amines
13%
Regioselectivity
11%
Rhodium
11%
Enantioselectivity
11%
Amides
11%
Carbon
10%
Naphthalene
10%
Functional groups
9%
Oxidants
9%
Alcohols
9%
Alkenylation
9%
Pharmaceutical Chemistry
8%
Sulfides
8%
Carboxylic acids
8%
Chemical activation
7%
Atoms
7%
Substrates
7%
Halogenation
7%
Cyclohexane
7%
Oxides
7%
Metals
7%
Lactams
7%
Biosynthetic Pathways
7%
Stereochemistry
7%
Carbonyl compounds
6%
Oxidation
6%
Cycloaddition
6%
Anthracene
6%
Lead compounds
6%
Dimerization
6%
Chirality
5%
Reagents
5%
Transition metals
5%
Borates
5%
Antibiotics
5%