Chemical Compounds
Nitroalkene
82%
Cross-Coupling Reaction
70%
Aldol Addition
58%
Cycloaddition
56%
Aldehyde
48%
Phosphoramide
48%
Reaction Yield
46%
Acetal
46%
Alkene
45%
Lewis Acid
40%
Catalyst
34%
Vinyl Ether
28%
Iodide
22%
Ketene
21%
Stereoselectivity
20%
Cyclization Reaction
20%
Total Synthesis
19%
Tetrabutylammonium Fluoride
19%
Allylation
18%
Transmetalation
18%
Palladium
17%
Base Catalysis
17%
Ether
17%
Chemistry
17%
Electrophile
15%
Bromide
15%
Anion
15%
Nazarov Cyclization
15%
Imine
13%
Silanols
13%
Alkylation
12%
Double Bond
12%
Allylic Alcohol
12%
Fluoride
11%
Ion
11%
Aldehyde Allylation
10%
Ring Closing Metathesis
10%
Stereochemistry
10%
Medicine & Life Sciences
Lewis Bases
77%
Palladium
70%
Cross Reactions
62%
3-hydroxybutanal
59%
Alkenes
45%
Cycloaddition Reaction
38%
Aldehydes
35%
Acetals
34%
phosphoramide
33%
Silicon
31%
Cyclization
31%
Lewis Acids
30%
Ethers
27%
Ketones
24%
Catalysis
20%
Bromides
20%
silanol
20%
tetrabutylammonium
19%
Iodides
17%
vinyl ether
14%
Styrenes
14%
ketene
13%
Esters
13%
Ions
12%
stannic chloride
12%
Carbon
12%
Kinetics
11%
Siloxanes
11%
Anions
11%
Salts
10%
Electrons
10%
Fluorides
9%
titanium tetrachloride
8%
silicon tetrachloride
8%
Phosphoramides
8%
Phosphorus
7%
Nitrogen
7%
benzaldehyde
6%
Alkylation
6%
Alcohols
6%
1,3-butadiene
6%
papulacandins
6%
Ligands
6%
potassium trimethylsilanolate
5%
disiloxane
5%
Polyenes
5%
Amides
5%
Temperature
5%
Chlorides
5%
Acids
5%
Engineering & Materials Science
Enantioselectivity
44%
Olefins
39%
Palladium
38%
Cycloaddition
35%
Catalysis
31%
Catalysts
30%
Nucleophiles
28%
Acids
24%
Addition reactions
20%
Silicon
18%
Chemical activation
16%
Ions
15%
Stereoselectivity
13%
Carbon
13%
Negative ions
11%
Alcohols
11%
Potassium
11%
Functional groups
11%
Atoms
10%
Rhodium
9%
Electrons
9%
Salts
8%
Substrates
7%
Amines
6%
Nuclear magnetic resonance
6%
Pyridine
6%
Conformations
5%
Molecules
5%
Spectroscopic analysis
5%
Styrene
5%
Sulfur
5%
Substitution reactions
5%