Chemical Compounds
Total Synthesis
100%
Mukaiyama Aldol Addition
61%
Silyl
52%
Occurrence in Nature
27%
Aldol Reaction
25%
Ciguatoxin
22%
Stereoselectivity
22%
Imide
21%
Cyclization Reaction
20%
Alkylation
13%
Tertiary Alcohol
12%
Stereochemistry
12%
Tyrosine Kinase Inhibitor
11%
Adduct
10%
Mitsunobu Reaction
9%
Acetal
9%
Condensation
9%
Carbon Atom
9%
Julia-Kocienski Olefination
9%
Trichostatin D
8%
Pentose Derivative
8%
Terpene
8%
Ketene
7%
Lactate
7%
Epoxide
7%
Application
7%
Reductive Coupling
7%
Leaf Like Crystal
7%
Epi-Cochlioquinone A
6%
Iodide
6%
Absolute Configuration
6%
Glycosylation
6%
Diastereomer
6%
Acid
6%
Ether
6%
Chemical Transformation
6%
Esterification
6%
Propionate
6%
Birch Reduction
6%
Stereoisomer
6%
Ugi Condensation
6%
Compound Isomer
6%
Oxidation Reaction
6%
Reaction Yield
5%
(+)-Menthone
5%
Lactonamycin
5%
Molecule
5%
Medicine & Life Sciences
3-hydroxybutanal
80%
Acetals
62%
Imides
20%
Cyclization
20%
Lewis Acids
19%
Biological Products
17%
Polyketides
16%
Alkylation
15%
khafrefungin
14%
hibarimicinone
14%
YCM 1008A
14%
1,25-dihydroxy-19-norvitamin D3
13%
eleutherobin
12%
Aldehydes
11%
tubelactomicin A
10%
lagunamycin
10%
trichostatin D
10%
Skeleton
9%
Lactones
9%
stannic chloride
8%
Esterification
8%
Carbon
8%
Cycloaddition Reaction
8%
Anhydrides
8%
2-methylbenzimidazole
7%
Halogenation
7%
Acids
7%
TMC-264
7%
BE 52440 A
7%
tabtoxinine
7%
Glycosylation
7%
Iodides
7%
alkoxyl radical
7%
aculeximycin
7%
lactonamycin
7%
ribonolactone
6%
alnumycin
6%
madindoline A
6%
src-Family Kinases
6%
cochlioquinone A
6%
acetylenic alcohol
6%
Anions
6%
Esters
6%
methyl acetoacetate
6%
mycocerosic acid
6%
Lactams
6%
Antitubercular Antibiotics
5%
benzanthrone
5%
ketene
5%