Chemical Compounds
Hydrindane
100%
Ring Formation
95%
Organoammonium Salt
77%
Indole Alkaloid
70%
Cyclization Reaction
68%
Tryptamine
58%
Terpenoid Indole Alkaloid
54%
Occurrence in Nature
53%
Decalin
47%
Ester
44%
Block Like Crystal
41%
Total Synthesis
40%
Enantioselectivity
39%
Vinylboronic Ester
37%
Ugi Condensation
35%
Catalyst
34%
Metallocene
32%
Cyanomethylation
32%
Primary Allylic Alcohol
31%
Cycloaddition
31%
Intramolecular Cyclization
30%
Cardenolides
29%
Tryptamines
28%
Anti Hepatitis
27%
Adduct
26%
Hydroarylation
26%
Tetrahydropyridine
26%
Intramolecular Cycloaddition
25%
Aryne
25%
Cyclohexane
24%
Henry Reaction
23%
Enyne
23%
Thioureas
23%
N-Bromosuccinimide
22%
Coupling Reaction
22%
Antimalarial
21%
Acrolein
21%
Nitrone
21%
Aldol Reaction
20%
Aryl Group
20%
Ammonium Salt
20%
Chemical Transformation
19%
1,3-cycloaddition
19%
Indoles
18%
Glyoxylate Ester
17%
Diels-Alder Reaction
17%
Ouabagenin
17%
Reaction Yield
17%
Hydrolysis
17%
Steroid
16%
Medicine & Life Sciences
Alkynes
89%
hydrindane
76%
Dihydropyridines
55%
Cyclization
55%
Titanium
47%
1,4-cyclohexadiene
37%
decalin
35%
3-hydroxybutanal
33%
Rhodium
32%
allyl alcohol
31%
Artemisinins
30%
Pyrrolidines
30%
Indole Alkaloids
29%
Indoles
29%
Thiourea
27%
tryptamine
26%
Tryptamines
26%
Cycloaddition Reaction
25%
artemisinine
23%
1,4-dihydropyridine
23%
Biomimetics
23%
n-butyllithium
19%
Amines
19%
Oxidants
19%
Skeleton
18%
Esters
18%
Biological Products
18%
Acceleration
17%
glyoxylic acid
17%
Hepacivirus
17%
decane
15%
Heterocyclic Compounds
15%
Electrons
14%
Nitriles
14%
Alkenes
14%
Cyclohexane
14%
Temperature
13%
Amino Acids
12%
Hexanes
12%
salicylaldehyde
11%
Bromosuccinimide
11%
Antimalarials
10%
Copper
9%
Imines
9%
Ligands
6%
Drug Development
5%
Hydrolysis
5%