catalyst - triethylamine

См. также в других словарях:

• Triethylamine — Triethylamine …   Wikipedia

• Triethylamine hydrochloride — Chembox new Name = Triethylamine hydrochloride IUPACName = Triethylamine hydrochloride ImageFile = Triethylamine hydrochloride.gif ImageSize = 200px ImageName = Chemical structure of triethylamine hydrochloride Section1 = Chembox Identifiers… …   Wikipedia

• Heck reaction — The Heck reaction (also called the Mizoroki Heck reaction)[1] is the chemical reaction of an unsaturated halide (or triflate) with an alkene and a base and palladium catalyst to form a substituted alkene.[2][3] Together with the other palladium… …   Wikipedia

• Oseltamivir total synthesis — concerns the total synthesis of the antiinfluenza drug oseltamivir marketed by Hoffmann La Roche under the trade name Tamiflu. Its commercial production starts from the biomolecule shikimic acid harvested from Chinese star anise with a limited… …   Wikipedia

• Trost asymmetric allylic alkylation — The Trost asymmetric allylic alkylation or Trost AAA or allylic asymmetric substitution is an organic reaction used in asymmetric synthesis. [Trost, B. M.; Fullerton, T. J. New synthetic reactions. Allylic alkylation. J. Am. Chem. Soc. 1973, 95 …   Wikipedia

• Synthèse totale de l'oseltamivir — Oseltamivir La synthèse totale de l oseltamivir correspond à la synthèse totale du principe actif antigrippal commercialisé par Hoffmann La Roche sous le nom de marque Tamiflu. Sa production commerciale commence à partir de l acide shikimique,… …   Wikipédia en Français

• 4-Dimethylaminopyridine — IUPAC name 4 Dimethylaminopyridine …   Wikipedia

• Esterification — is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials, and often have a characteristic pleasant …   Wikipedia

• Sonogashira coupling — In organic chemistry, a Sonogashira coupling is a coupling reaction of terminal alkynes with aryl or vinyl halides. This reaction was first reported by Kenkichi Sonogashira and Nobue Hagihara in 1975. [cite journal author = K. Sonogashira, Y.… …   Wikipedia

• Azide alkyne Huisgen cycloaddition — The Azide Alkyne Huisgen Cycloaddition is a 1,3 dipolar cycloaddition between an azide and a terminal or internal alkyne to give a 1,2,3 triazole. Rolf Huisgen[1] was the first to understand the scope of this organic reaction. American chemist K …   Wikipedia

• Ethylamine — Ethylamine[1] …   Wikipedia