trifluoromethanesulfonic acid has been researched along with methanol in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (50.00) | 29.6817 |
| 2010's | 3 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Broker, GA; Holbrey, JD; Klingshirn, MA; Rogers, RD; Shaughnessy, KH | 1 |
| Brown, RS; Neverov, AA; Tsang, JS | 1 |
| Bowers, AA; Crich, D; Nokami, T; Shibuya, A; Suga, S; Tsuyama, H; Yoshida, J | 1 |
| Chen, Z; Wu, J; Yu, X | 1 |
| Whitfield, DM | 2 |
6 other study(ies) available for trifluoromethanesulfonic acid and methanol
| Article | Year |
|---|---|
Polar, non-coordinating ionic liquids as solvents for the alternating copolymerization of styrene and CO catalyzed by cationic palladium catalysts.
Topics: Carbon Monoxide; Imides; Mesylates; Methanol; Molecular Weight; Palladium; Polymers; Pyridinium Compounds; Styrene | 2002 |
Billion-fold acceleration of the methanolysis of paraoxon promoted by La(OTf)3 in methanol.
Topics: Chemical Warfare Agents; Insecticides; Kinetics; Lanthanum; Magnetic Resonance Spectroscopy; Mesylates; Methanol; Paraoxon | 2003 |
Electrochemical generation of glycosyl triflate pools.
Topics: Carbohydrates; Electrochemistry; Galactose; Glycosides; Mannose; Mesylates; Methanol; Nuclear Magnetic Resonance, Biomolecular; Oxidation-Reduction; Sulfhydryl Compounds | 2007 |
Silver triflate and N-heterocyclic carbene co-catalyzed reaction of N'-(2-alkynylbenzylidene)hydrazide, methanol with alpha,beta-unsaturated aldehyde.
Topics: Aldehydes; Azides; Catalysis; Heterocyclic Compounds; Isoquinolines; Mesylates; Methane; Methanol; Molecular Structure; Stereoisomerism | 2010 |
Plausible Transition States for glycosylation reactions.
Topics: Glycosides; Glycosylation; Lithium; Mesylates; Methanol; Methylene Chloride; Models, Chemical; Models, Molecular; Molecular Conformation; Oxygen; Quantum Theory; Stereoisomerism; Thermodynamics | 2012 |
Complications of modeling glycosylation reactions: can the anomeric conformation of a donor determine the glycopyranosyl oxacarbenium ring conformation?
Topics: Cations; Electrons; Glycosides; Glycosylation; Hydrogen Bonding; Mesylates; Methanol; Models, Chemical; Models, Molecular; Molecular Conformation; Quantum Theory; Stereoisomerism; Thermodynamics; Thiosulfonic Acids | 2012 |