Chemical Compounds
Total Synthesis
100%
Allylic Amination
78%
Occurrence in Nature
74%
Ylide
53%
1,2 Rearrangement
47%
Amine
43%
Alkene
40%
Grignard Reagent
38%
Iodonium
38%
Diastereoselectivity
37%
Pyran
36%
Chemical Transformation
32%
Cycloaddition
32%
Allylic Alkylation
29%
Substitution Reaction
29%
Alkaloid
29%
Anthraquinone
28%
Aza-Diels-Alder Reaction
28%
Aryne
25%
Molecule
24%
Catalyst
23%
N-Oxide
22%
Meisenheimer N-Oxide Rearrangement
22%
Reaction Yield
21%
Allylic Alcohol
21%
Aromatic Structure
21%
Sulfinamidine
21%
Cyclopropane
20%
Casopitant
20%
Regioselectivity
19%
Hauser-Kraus Annulation
18%
Ammonium Ylide
18%
Acid
17%
Neurokinin-1 Receptor Antagonist
17%
Lewis Acid
16%
Carbon Atom
16%
Meisenheimer Rearrangement
16%
Enantioselectivity
16%
Thiophene-2-Carboxylic Acid
15%
Aza-Claisen Rearrangement
15%
N-Acetylhexosamine
15%
Fluoride
15%
Mammalian Cell
14%
Danishefsky Cycloaddition
14%
Heterodimerization
14%
Benzannulation
13%
Diazirine
13%
Pericyclic Reaction
13%
Tetrahydropyridine
13%
Medicine & Life Sciences
endothelial PAS domain-containing protein 1
76%
Palladium
74%
Amination
59%
Biological Products
48%
Amines
44%
Alkenes
44%
Lewis Acids
36%
Copper
34%
Cycloaddition Reaction
31%
Pyrans
31%
3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
30%
Metals
27%
hydronium ion
27%
Alkylation
25%
indole
24%
saudin
24%
Ammonium Compounds
24%
Acids
23%
rubellin
23%
aurantioclavine
23%
Silicon
22%
Aldehydes
22%
Peptic Esophagitis
22%
Ligands
22%
Cyclopropanes
21%
Alkaloids
20%
sparstolonin B
20%
2-thiophene carboxylic acid
20%
Cyclic Amino Acids
18%
Carbon
17%
sulfuryl fluoride
17%
Rhodium
16%
Anthraquinones
16%
benzothiophene
16%
Phosphotransferases
16%
Iodides
16%
phosphine
16%
allyl alcohol
16%
Hydrocarbons
15%
Pyrrolidines
15%
Lobeline
15%
Indoles
15%
Pyruvate Dehydrogenase (Acetyl-Transferring) Kinase
14%
Hydrazones
14%
Cyclization
14%
Sulfones
14%
Imines
14%
glyoxylic acid
13%
tryptamine
13%
Density Functional Theory
13%
Engineering & Materials Science
Reagents
51%
Olefins
50%
Alkaloids
50%
Catalysts
49%
Alkylation
48%
Copper
45%
Amines
39%
Functional groups
36%
Amination
35%
Cyclization
33%
Palladium
31%
Nucleophiles
30%
Regioselectivity
28%
Cycloaddition
25%
Substrates
24%
Allylation
23%
Ligands
20%
Alcohols
20%
Acids
19%
Molecules
19%
Enantioselectivity
19%
Sulfonamides
17%
Fluorination
15%
Metals
15%
Carbon
14%
Rhodium
14%
Photocatalysts
14%
Density functional theory
14%
Isomerization
13%
Aldehydes
13%
Sulfur
13%
Substitution reactions
12%
Butane
12%
Oxidation
11%
Byproducts
9%
Catalysis
9%
Oxides
8%
Derivatives
7%
Silicon
7%
Nitrogen
7%
Amides
7%
Chemical activation
7%
Iridium
6%
Transition metals
6%
Metal ions
6%
Energy transfer
5%
Carbonates
5%
Discrete Fourier transforms
5%