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  2. Fluoroalcohol - Wikipedia

    en.wikipedia.org/wiki/Fluoroalcohol

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  3. Fluorotelomer alcohol - Wikipedia

    en.wikipedia.org/wiki/Fluorotelomer_alcohol

    Aerobic biotransformation pathways of 8:2 FTOH in soil [10] The fluorotelomer alcohols 6:2 FTOH and 8:2 FTOH have been found to be estrogenic. [11] 10:2 fluorotelomer alcohol (10:2 FTOH) The atmospheric oxidation of fluorotelomer alcohols can also result in anthropogenic perfluorinated carboxylic acids. [12]

  4. 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.

  5. 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.

  6. Metabolic pathway - Wikipedia

    en.wikipedia.org/wiki/Metabolic_pathway

    An anabolic pathway is a biosynthetic pathway, meaning that it combines smaller molecules to form larger and more complex ones. [ 10 ] : 570 An example is the reversed pathway of glycolysis, otherwise known as gluconeogenesis , which occurs in the liver and sometimes in the kidney to maintain proper glucose concentration in the blood and supply ...

  7. Nonafluoro-tert-butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Nonafluoro-tert-butyl_alcohol

    Nonafluoro-tert-butyl alcohol (IUPAC name: 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-ol) is a fluoroalcohol. It is the perfluorinated analog of tert-butyl alcohol. Notably, as a consequence of its electron withdrawing fluorine substituents, it is very acidic for an alcohol, with a pK a value of 5.4, similar to that of a carboxylic acid.

  8. Hexafluoro-2-propanol - Wikipedia

    en.wikipedia.org/wiki/Hexafluoro-2-propanol

    Hexafluoro-propan-2-ol is a speciality solvent for organic synthesis, particularly for reactions involving oxidations and strong electrophiles. For example, HFIP enhances the reactivity of hydrogen peroxide as applied to Baeyer-Villiger oxidation of cyclic ketones. [ 1 ]

  9. Glyoxylate cycle - Wikipedia

    en.wikipedia.org/wiki/Glyoxylate_cycle

    The glyoxylate cycle, a variation of the tricarboxylic acid cycle, is an anabolic pathway occurring in plants, bacteria, protists, and fungi. The glyoxylate cycle centers on the conversion of acetyl-CoA to succinate for the synthesis of carbohydrates . [ 1 ]