triphenylphosphine oxide

triphenylphosphine oxide
Химия: трифенилфосфиноксид

Универсальный англо-русский словарь. . 2011.

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  • 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


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