Chemical Compounds
Allylation
100%
Total Synthesis
91%
Ring Closing Metathesis
76%
Ether
71%
Cyclic Ether
59%
Aldehyde
56%
Polycyclic Ether
49%
Ciguatoxin CTX3C
44%
Cyclization Reaction
37%
Brevetoxin B
36%
Lewis Acid
35%
Triflate
34%
Cyclic Structure
34%
Acetal
28%
2-Deoxy-D-Ribose
27%
Occurrence in Nature
27%
Stannane
27%
Absolute Configuration
25%
Diastereomer
24%
Stereoselectivity
23%
Macrolactonization
22%
Reaction Yield
19%
Polyol
19%
1H NMR Data
18%
Hetero-Michael Addition
17%
Intramolecular Cyclization
17%
Yessotoxin
16%
Diastereoselectivity
16%
Chemical Transformation
15%
Allylboration
15%
Julia-Kocienski Olefination
15%
13C NMR Data
15%
Alkyne
14%
Antifouling
12%
Palladium
12%
Substance Spectroscopy
12%
Carbon Atom
11%
Ketene
11%
Stereochemistry
10%
Imine
10%
Brown
10%
Macrolide Antibiotic Agent
9%
Sharpless Asymmetric Dihydroxylation
9%
Alcohol
9%
Acetal Elimination Reaction
9%
Evans Reaction
9%
Reductive Cyclization
9%
L-Glutamic Acid
8%
Cadiot-Chodkiewicz Coupling
8%
Alkylation
8%
Medicine & Life Sciences
Ether
77%
gambierol
76%
Cyclization
69%
Aldehydes
56%
Cyclic Ethers
49%
Lewis Acids
44%
ciguatoxin 3C
43%
Acetals
35%
Ribose
31%
Ethers
29%
Palladium
25%
yessotoxin
19%
stannane
19%
brevetoxin B
18%
Tin
16%
Alkynes
16%
Carbon
15%
Alkylation
14%
ketene
13%
trifluoromethanesulfonic acid
12%
Acids
12%
polyol
12%
propadiene
11%
Alcohols
11%
Hydrogenation
11%
Carboxylic Acids
10%
Biological Products
10%
Alkenes
10%
pyrrolidine
10%
Imines
10%
titanium tetrachloride
9%
Benzoic Acid
9%
geraniol
9%
nakiterpiosin
8%
dactylolide
8%
neopeltolide
8%
Cycloaddition Reaction
8%
Macrolides
8%
laurencin
8%
thermospermine
8%
preussin
7%
brevicomin
7%
dithiane
7%
Thoracica
7%
Carbon-13 Magnetic Resonance Spectroscopy
7%
penitricin C
7%
Skeleton
6%
Esters
6%
candidin
6%
3-hydroxybutanal
6%