Chemical Compounds
[2,3]-Wittig Rearrangement
100%
[1,2]-Wittig Rearrangement
91%
Chirality
58%
Carbanion
47%
Cyclization Reaction
33%
Alkyne
31%
Stannane
30%
Enantiomer
29%
Ether
28%
Lithiation
26%
Chemical Transformation
26%
Diastereoselectivity
24%
Stereochemistry
24%
Oxazoline
21%
Alcohol
21%
Wittig Rearrangement
20%
Ozone
20%
Cyclic Amide
20%
Amide
20%
Acetal
19%
Enantioselectivity
19%
Transmetalation
19%
Cinchonine
18%
Silyl
18%
Oxidation Reaction
17%
Protomycinolide IV
17%
Lactol
17%
Cinchonidine
17%
Cycloalkyne
17%
Silyl Group
16%
Reaction Yield
16%
Carbon Atom
16%
Grignard Reagent
15%
Erythronolide A
15%
Cyclic Ether
15%
Zaragozic Acid A
15%
Molecule
15%
Nucleophilic Addition
14%
Chromenes
14%
Carbonyl Compound
14%
Alkene
14%
Butyllithium
13%
Block Like Crystal
13%
Glycogen
13%
Azide
13%
Cyclic Structure
12%
Oxy-Cope Rearrangement
12%
Triol
12%
Enantiopurity
12%
Enyne
12%
Medicine & Life Sciences
2,5-dimethylcelecoxib
50%
1-((3,5-dichloro)-2,6-dihydroxy-4-methoxyphenyl)-1-hexanone
41%
Cyclization
39%
stannane
37%
pinacol
34%
Glycogen Synthase Kinase 3
27%
Alkynes
26%
Ethers
25%
butyllithium
24%
Cyclic Ethers
24%
Amides
24%
protomycinolide IV
21%
Carbon
18%
Celecoxib
17%
Ether
16%
Lactones
15%
Ligands
15%
C-glycoside
15%
Alkenes
14%
Alcohols
14%
Furans
13%
Imides
13%
allyl alcohol
13%
Cycloaddition Reaction
13%
High Pressure Liquid Chromatography
13%
Ketones
12%
propylene
12%
Acids
12%
Lewis Acids
11%
Catenins
11%
Azides
11%
quinone methide
11%
Cyclin D1
10%
Nitrogen
10%
Thermodynamics
9%
Glycosides
9%
Aldehydes
9%
erythronolide A
9%
methoxymethylbenzene
9%
Density Functional Theory
9%
X-Rays
9%
helicenes
9%
Complement Activation
9%
antibiotic 1233A
9%
3'-azido-2',3'-dideoxythymidine 5'-H-phoshonate
8%
Lithium
8%
Metals
8%
sulfilimine
8%
bicyclo(3.1.0)hexane
8%
phthalan
8%
Engineering & Materials Science
Chirality
35%
Cycloaddition
32%
Glycosides
22%
Cyclization
21%
Ligands
20%
Ethers
20%
Enantioselectivity
18%
Dimers
18%
Oxidation
17%
Porphyrins
17%
Complexation
16%
Substitution reactions
16%
Derivatives
13%
Nucleophiles
12%
Molecules
12%
Alcohols
12%
Olefins
12%
Enantiomers
11%
Stereochemistry
11%
Acids
11%
Negative ions
10%
Iron
10%
Peptides
10%
Silanes
10%
Ozone
10%
Column chromatography
10%
Reagents
9%
Carbonyl compounds
9%
Discrete Fourier transforms
8%
Hydrosilylation
8%
Silicon
7%
Nitrogen
7%
X ray crystallography
7%
Epoxidation
7%
Esters
6%
Oxygen
6%
Atoms
6%
High performance liquid chromatography
6%
Amides
6%
Polysaccharides
5%
Copolymerization
5%
Iodine
5%
Peroxides
5%
Palladium
5%
Self assembly
5%
Ethane
5%
Heptane
5%
Alkenylation
5%