Pharmacology, Toxicology and Pharmaceutical Science
Nucleophile
100%
Tetrafluoroborate
100%
Pyrimidine
100%
Nitrogen 15
45%
Pyrimidine Derivative
45%
Sulfate
36%
Acetic Acid Derivative
18%
Open-Chain Compound
18%
Acrylamide Derivative
18%
Carbon 13
18%
Cyanamide
9%
Benzene Derivative
9%
Potassium Hydroxide
9%
Triethyloxonium Tetrafluoroborate
9%
Pyridine Derivative
9%
Amidinium
9%
Carbon 14
9%
Table Salt
9%
Carbene
9%
Imine
9%
Chemistry
Ethyl
100%
Nucleophile
100%
Pyrimidinium Salt
27%
Hydrogen
16%
Ethoxylation
16%
Ring Opening Reaction
11%
Acetyl
11%
Acrylamide
11%
1H NMR Spectroscopy
11%
Space Group
11%
13C NMR Spectroscopy
11%
4-Phenylpyrimidine
11%
2-Methylpyridine
11%
Methyl Sulfate(1-)
11%
Nucleophilic Substitution
11%
Crystal Structure
5%
Condensation
5%
Recyclization
5%
Rearrangement Reaction
5%
Ring Cleavage
5%
Sodium Ethoxide
5%
Demethylation
5%
Potassium Hydroxide
5%
Molecular Structure
5%
Sulfate
5%
Methyl Sulfate
5%
Ethoxy Group
5%
Cyanamide
5%
Dimroth Rearrangement
5%
Table Salt
5%
formation
5%
amination
5%
Carbene
5%
Imine
5%