lactone reactions


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  • What is the chemistry of lactones?

    lactone, any of a class of cyclic organic esters, usually formed by reaction of a carboxylic acid group with a hydroxyl group or halogen atom present in the same molecule.

  • The proposed mechanism involves the intermediacy of the corresponding aldehyde resulting from a retro-aldol cleavage of the dicyanovinyl group; this aldehyde can then undergo an intramolecular aldol reaction with the enolate <1983BCJ1219> (Scheme 64).

  • What is the mechanism of action of lactone?

    Macrocyclic lactones act as GABA agonists and also bind to glutamate-gated chloride channels in nerve and muscle cells of invertebrates.
    In both cases, these actions block the transmission of neuronal signals of the parasites, which are either paralyzed and expelled out of the body, or starved helmints.

  • What is the reaction of lactone formation?

    Lactones are formed by intramolecular esterification of the corresponding hydroxycarboxylic acids, which takes place spontaneously when the ring that is formed is five- or six-membered.
    Lactones with three- or four-membered rings (α-lactones and β-lactones) are very reactive, making their isolation difficult.

  • Lactone's hydrolysis condensation reaction is a reversible reaction with equilibrium. Lithium aluminium hydride reduces lactones to diols. The reaction involves the breaking of the ester bond and then the carboxylic acid group is reduced to the alcohol group. Polyesters are formed by lactones.
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