Medicine & Life Sciences
agelastatin A
100%
Cyclization
41%
Alkaloids
34%
CP 263114
34%
Acetogenins
29%
platencin
28%
Nitrogen
22%
Protein Carbamylation
21%
Benzethonium
20%
Lactones
19%
Oxazolidinones
18%
Stereoisomerism
18%
ligudentatol
17%
clavilactone B
17%
Carbon
16%
Biological Products
16%
7-oxabicyclo(2.2.1)heptane
16%
Illudane
15%
mesembrine
14%
pantolactone
14%
Amines
13%
Osteopontin
13%
glycidol
12%
Brain Neoplasms
12%
indacrinone
12%
Samarium
12%
Cell Line
12%
Structure-Activity Relationship
11%
Amides
11%
p21(ras) farnesyl-protein transferase
11%
Epichlorohydrin
11%
Benzazepines
11%
N-methylpyrrolidone
11%
alkoxyl radical
11%
Growth
11%
Central Nervous System
10%
Air
10%
2-aminoethoxydiphenyl borate
10%
Alkenes
10%
Anhydrides
10%
Isocyanates
10%
Palladium
10%
Carbon Cycle
10%
Muscarine
10%
Pharmacokinetics
9%
Extensively Drug-Resistant Tuberculosis
9%
Glycols
9%
Agelas
9%
Urea
9%
Porifera
9%
Chemical Compounds
Total Synthesis
92%
Alkaloid
44%
Occurrence in Nature
32%
Radical Cyclization
31%
Chemical Transformation
29%
Platencin
28%
Cyclization Reaction
28%
Conduritol
22%
Oxazolidinone
21%
Grob Fragmentation
21%
Sharpless Asymmetric Dihydroxylation
18%
Cyclohexenone
18%
Aldehyde
18%
Cyclic Structure
18%
Nitrogen
15%
Sharpless Reaction
14%
Structure-Activity Relationship
14%
2,5-furandimethanol
13%
Stereoisomer
13%
Isocyanate
13%
Dihydroxylation
13%
Free Radical
13%
N-Methylpyrazole
12%
Diastereomer
12%
Demethoxycarbonylation
12%
Wharton Fragmentation
11%
(R)-Pantolactone
11%
Muscarine
11%
Dienone-Phenol Rearrangement
10%
Carbon Atom
10%
Benzofuran
10%
Cyclohex-2-Enone
10%
Double Bond
10%
cyclohexa-1,3-diene
10%
Aminocarbonylation
10%
1,4-dioxane
10%
Pharmacokinetics
9%
Indanone
9%
Reaction Yield
9%
Asymmetric Dihydroxylation
9%
N-Chlorosuccinimide
9%
Cytotoxin
9%
Ethyl
9%
Lactone
9%
Polycyclic Compound
9%
Absolute Configuration
9%
Tertiary Amide
9%
Optical Yield
9%
Purity
9%
Bacteriostatic
8%