- triphenylphosphine oxide
- Химия: трифенилфосфиноксид
Универсальный англо-русский словарь. Академик.ру. 2011.
Универсальный англо-русский словарь. Академик.ру. 2011.
Triphenylphosphine oxide — Triphenylphosphine oxide … Wikipedia
Triphenylphosphine — Chembox new Name = Triphenylphosphine ImageFile = Triphenylphosphine structure.svg ImageName = Triphenylphosphine ImageFile1 = Triphenylphosphine ray 3D balls.png ImageName1 = Ball and stick model of the triphenylphosphine molecule IUPACName =… … Wikipedia
Triphenylphosphine sulfide — chembox new ImageFile = Triphenylphosphine sulfide 2D skeletal.png ImageSize = ImageFile1 = Triphenylphosphine sulfide 3D balls.png ImageSize1 = IUPACName = triphenylthioxophosphorane OtherNames = Section1 = Chembox Identifiers CASNo= 3878 45 3… … Wikipedia
Phosphine oxide — Phosphine oxide, organophosphorus compounds with the formula OPR3. Phosphines are often air sensitive, and are often oxidized to phosphine oxides on prolonged storage.ee also*Triphenylphosphine oxide *Organophosphorus *Phosphine PR3 *Phosphinite… … Wikipedia
Ethylene oxide — Oxirane redirects here. For oxiranes as a class of molecules, see epoxide. Ethylene oxide … Wikipedia
Oxotrichlorobis(triphenylphosphine)rhenium(V) — IUPAC name Trichlorid … Wikipedia
Organophosphorus — compounds are degradable organic compounds containing carbon–phosphorus bonds (thus excluding from phosphate and phosphite esters, which lack such kind of bonding), used primarily in pest control as an alternative to chlorinated hydrocarbons that … Wikipedia
Mitsunobu reaction — The Mitsunobu reaction is an organic reaction that converts an alcohol into a variety of functional groups, such as an ester, using triphenylphosphine and an azodicarboxylate such as diethyl azodicarboxylate (DEAD) or diisopropyl azodicarboxylate … Wikipedia
Staudinger reaction — The Staudinger reaction or Staudinger reduction is a chemical reaction in which the combination of an azide with a phosphine or phosphite produces an iminophosphorane intermediate [Staudinger, H.; Meyer, J. Helv. Chim. Acta 1919, 2 , 635.]… … Wikipedia
Pyridine — Pyridine … 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