allylpalladium

allylpalladium

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  • Allylpalladium chloride dimer — Chembox new Name = Allylpalladium(II) chloride dimer ImageFile1 = Allylpalladium chloride dimer 3D balls.png ImageFile2 = AllPdCl 2.png IUPACName = Allylpalladium(II) chloride dimer OtherNames = Allylpalladium chloride dimer bis(allyl)di μ chloro …   Wikipedia

  • Organopalladium — chemistry is a branch of organometallic chemistry that deals with organic palladium compounds and their reactions. Palladium is often used as a catalyst in the reduction of alkenes and alkynes with hydrogen. This process involves the formation of …   Wikipedia

  • APC — or Apc or may refer to:Biology* Antigen presenting cell in medicine/immunology * APC (gene), a human gene that is classified as a tumor suppressor gene * APC (protein), a human cancer critical protein (product of APC (gene)) * Anaphase promoting… …   Wikipedia

  • Allyl chloride — Allyl chloride …   Wikipedia

  • Hiyama coupling — In organic chemistry, a Hiyama coupling is a palladium or nickel catalyzed cross coupling reaction of organosilanes with organic halides or triflates. Hiyama couplings were first reported by Yasuo Hatanaka and Tamejiro Hiyama in 1988 [ Cross… …   Wikipedia

  • Kinetic resolution — In kinetic resolution, two enantiomers show different reaction rates in a chemical reaction, thereby creating an excess of the less reactive enantiomer.[1] This excess goes through a maximum and disappears on full completion of the reaction.… …   Wikipedia

  • Silyl enol ether — Silyl enol ethers in organic chemistry are a class of organic compounds sharing a common functional group composed of an enolate bonded through its oxygen terminus to an organosilicon group.Silyl enol ethers are important intermediates in organic …   Wikipedia

  • 107-05-1 — Chlorure d allyle Chlorure d allyle …   Wikipédia en Français

  • Chlorure d'allyl — Chlorure d allyle Chlorure d allyle …   Wikipédia en Français

  • Chlorure d'allyle — Chlorure d allyle …   Wikipédia en Français

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