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  2. Fluorotelomer alcohol - Wikipedia

    en.wikipedia.org/wiki/Fluorotelomer_alcohol

    The synthesis of fluorotelomer alcohols requires a varying number of tetrafluoroethylene monomers that form an oligomer with a pentafluoroethyl iodide telogen. The fluorinated iodide then undergoes an addition with ethylene to form an organoiodine compound with increased synthesis possibilities. [ 1 ]

  3. Template:Metabolic pathways - Wikipedia

    en.wikipedia.org/wiki/Template:Metabolic_pathways

    This page is the template for the metabolic pathways template. This template should be used to illustrate the general 'shape' of metabolism within the cell. This template is part of the Metabolic Pathways task force. This template has been largely superseded by {{Metabolic metro}} but is kept as an archive

  4. Fluoroalcohol - Wikipedia

    en.wikipedia.org/wiki/Fluoroalcohol

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  5. Metabolic pathway - Wikipedia

    en.wikipedia.org/wiki/Metabolic_pathway

    However, side products are considered waste and removed from the cell. [2] Different metabolic pathways function in the position within a eukaryotic cell and the significance of the pathway in the given compartment of the cell. [3] For instance, the electron transport chain and oxidative phosphorylation all take place in the mitochondrial membrane.

  6. Pharmacology of ethanol - Wikipedia

    en.wikipedia.org/wiki/Pharmacology_of_ethanol

    All organisms produce alcohol in small amounts by several pathways, primarily through fatty acid synthesis, [70] glycerolipid metabolism, [71] and bile acid biosynthesis pathways. [72] Fermentation is a biochemical process during which yeast and certain bacteria convert sugars to ethanol, carbon dioxide, as well as other metabolic byproducts.

  7. 2-Fluoroethanol - Wikipedia

    en.wikipedia.org/wiki/2-Fluoroethanol

    2-Fluoroethanol was originally synthesized by treating 2-chloroethanol with potassium fluoride, in a simple Finkelstein reaction. [5] The product has a lower boiling point that the starting material and may be conveniently isolated by distillation.

  8. 2,2,2-Trifluoroethanol - Wikipedia

    en.wikipedia.org/wiki/2,2,2-Trifluoroethanol

    It is classified as a hard Lewis acid and its acceptor properties are discussed in the ECW model yielding E A = 2.07 and C A = 1.06. TFE can be used in biochemical experiments to stabilize alpha helix. [7] [8] There are also stable beta sheets in TFE, suggesting that TFE stabilizes the secondary structure the sequence has a preference for. [8]

  9. Flavin adenine dinucleotide - Wikipedia

    en.wikipedia.org/wiki/Flavin_adenine_dinucleotide

    Warburg's work with linking nicotinamide to hydride transfers and the discovery of flavins paved the way for many scientists in the 40s and 50s to discover copious amounts of redox biochemistry and link them together in pathways such as the citric acid cycle and ATP synthesis.