Chemical Compounds
Diels-Alder Reaction
57%
Meso Isomer
44%
Stereochemistry
41%
Undecane
40%
Epoxide
35%
Dihydrofuran
27%
Enol Ether
24%
Suzuki Coupling
23%
Silanes
22%
Ring Opening Reaction
22%
Grignard Reagent
21%
Photooxidation
20%
Cross-Coupling Reaction
20%
Diastereoselectivity
19%
Acetal
19%
Substitution Reaction
18%
Diol
18%
Macrocycle
18%
Communication
18%
Lewis Acid
17%
Ligand
17%
Nucleophile
17%
Alkylation
17%
Occurrence in Nature
16%
Reaction Yield
16%
Halide
15%
Zeolite
15%
Toluene
14%
Condensation
14%
Ethyl
14%
Aldehyde
13%
Catalysis
12%
Electric Field
12%
Thermodynamics
12%
Nonane
11%
Chloride
11%
Dioxygen
11%
Electron Particle
10%
Cyclohexene
10%
Product Distribution
10%
Stereoselectivity
9%
Cyclic Structure
9%
Application
7%
Bronsted Acid
6%
Chemical Transformation
6%
Catalyst
6%
Oxide
5%
Medicine & Life Sciences
Cycloaddition Reaction
100%
Epoxy Compounds
80%
Pyrones
70%
oxadecalin
51%
2-methyl-2-propen-1-ol
51%
spiroketal
40%
Lewis Acids
38%
3-hydroxybutanal
36%
Pyrans
33%
Electrons
31%
Cyclization
30%
Silanes
29%
Ligands
28%
Ketones
25%
Cobalt
23%
titanium isopropoxide
21%
Chlorides
21%
Titanium
20%
cyclohexene oxide
19%
Oxygen
14%
Cross Reactions
12%
Ether
11%
Iron
8%
phomactin A
6%
Physics & Astronomy
Diels-Alder reactions
34%
stereochemistry
30%
epoxy compounds
28%
synthesis
28%
dienes
28%
photooxidation
27%
xylene
26%
zeolites
22%
toluene
21%
entry
21%
products
19%
selectivity
18%
templates
18%
cations
16%
routes
16%
preparation
14%
acids
14%
oxygen
13%
rings
13%
electric fields
6%