Chemical Compounds
Ring Closing Metathesis
100%
Cross Metathesis
58%
Reaction Yield
50%
Alkene
43%
Cycloaddition
43%
Aza-Michael Addition
42%
Ring Opening Reaction
41%
Allylation
41%
Formate
39%
Hydrogenation
37%
Aldehyde
35%
Oxazoline
34%
Bortezomib
34%
Palladium
32%
Michael Addition
31%
Yamaguchi Esterification
30%
Reduction
30%
Enantioselectivity
30%
Sulfur Ylide
30%
Pericyclic Reaction
29%
1H-Isochromene
29%
Hydrobromide
27%
Total Synthesis
26%
Phosphine
26%
Stereochemistry
25%
Cyclization Reaction
25%
Acetal
25%
Ester
25%
1,2,3-triazole
24%
Acid
22%
Enone
22%
Cyclopropane
22%
Ligand
22%
Alkyne
21%
Alcohol
20%
Diastereoselectivity
20%
Benzyl Ether
20%
Carboxylic Acid
19%
Zoapatanol
19%
(-)-Quebrachamine
19%
Adduct
19%
Lactone
19%
Antiapoptotic
19%
Indole
19%
Diastereomer
18%
Azide
18%
Thioester
17%
Cannabinoid 1 Receptor Antagonist
17%
Corey-Chaykovsky Ring Formation
17%
Aminodiol
17%
Medicine & Life Sciences
Triazoles
69%
Cycloaddition Reaction
67%
Palladium
59%
Bortezomib
49%
1,5-hexadiene
46%
Aziridines
40%
Protein Phosphatase 2
39%
triphenylphosphine
39%
Hydrogenation
37%
Alkenes
37%
Acetogenins
36%
Cyclization
34%
Hepatocellular Carcinoma
32%
Apoptosis
32%
Azides
28%
70-kDa Ribosomal Protein S6 Kinases
27%
Ligands
25%
Alkynes
24%
Prostatic Neoplasms
24%
zoapatanol
24%
Ethers
23%
pachastrissamine
23%
Lactones
23%
Indenes
22%
C-galactosylceramide
22%
tigatuzumab
22%
squamocin
21%
Pyrroles
20%
ethyl lactate
20%
Human Activities
20%
PC-3 Cells
20%
Phosphatidylinositol 3-Kinases
20%
Isoindoles
20%
KRN 7000
19%
Autophagy
19%
decalin
19%
phthalide
19%
Benzene
19%
C-glycoside
18%
Alcohols
18%
Cannabinoid Receptor Antagonists
18%
Sulfur
18%
pyrroline
17%
Furans
17%
Acetals
17%
phosphine
17%
p-aminophenylarsine oxide
16%
Iridium
16%
tetrahydrofuran
16%
Ruthenium
16%
Physics & Astronomy
synthesis
98%
metathesis
60%
apoptosis
46%
cancer
38%
hexadiene
37%
rings
31%
adducts
31%
indoles
30%
phosphines
27%
tetrahydrofuran
27%
inhibitors
26%
cells
25%
alcohols
23%
acids
23%
Michael reaction
22%
ligands
20%
oxidation
20%
ketones
19%
products
19%
sulfur
19%
trienes
18%
Diels-Alder reactions
17%
closing
17%
congeners
17%
acetals
17%
indene
17%
methylene
17%
piperidine
16%
alkylation
16%
alkynes
16%
hydrogenation
16%
glucosides
16%
palladium
16%
catalysis
15%
stereochemistry
15%
cyclopropane
15%
lactates
14%
epoxy compounds
14%
aldehydes
14%
carboxylic acids
14%
pyrroles
14%
dienes
14%
spindles
13%
dehydrogenation
13%
rhenium
13%
chloroform
12%
catalysts
12%
cyclohexane
11%
death
11%
phosphorylation
11%