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  2. Lactol - Wikipedia

    en.wikipedia.org/wiki/Lactol

    In organic chemistry, a lactol is a functional group which is the cyclic equivalent of a hemiacetal (−CH(OH)O−) or a hemiketal (>C(OH)O−). The compound is formed by the intramolecular , nucleophilic addition of a hydroxyl group ( −OH ) to the carbonyl group ( C=O ) of an aldehyde ( −CH=O ) or a ketone ( >C=O ).

  3. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    Right: a lactol of fructose, a cyclic hemiketal. Hemiacetals commonly exist in nature as aldoses such as glucose , and hemiketals commonly exist in nature as ketoses such as fructose . The favorability of the formation of a strain-free six-membered ring and the electrophilicity of an aldehyde combine to strongly favor the acetal form.

  4. HCN channel - Wikipedia

    en.wikipedia.org/wiki/HCN_channel

    HCN channels are regulated by both intracellular and extracellular molecules [clarification needed], but most importantly, by cyclic nucleotides (cAMP, cGMP, cCMP). [9] [10] [11] Binding of cyclic nucleotides lowers the threshold potential of HCN channels, thus activating them. cAMP is a primary agonist of HCN2 while cGMP and cCMP may also bind ...

  5. Fétizon oxidation - Wikipedia

    en.wikipedia.org/wiki/Fétizon_oxidation

    This also allows for a classic use of Fétizon's reagent to form lactones from a primary diol. By oxidizing one of the alcohols to an aldehyde, the second alcohol equilibrates with the aldehyde to form a lactol which is reacted quickly with more Fétizon's reagent to trap the cyclic intermediate as a lactone. [8]

  6. Cyclic nucleotide–gated ion channel - Wikipedia

    en.wikipedia.org/wiki/Cyclic_nucleotide–gated...

    Cyclic nucleotide–gated ion channels or CNG channels are ion channels that function in response to the binding of cyclic nucleotides.CNG channels are nonselective cation channels that are found in the membranes of various tissue and cell types, and are significant in sensory transduction as well as cellular development.

  7. Lactone - Wikipedia

    en.wikipedia.org/wiki/Lactone

    Lactones are usually named according to the precursor acid molecule (aceto = 2 carbon atoms, propio = 3, butyro = 4, valero = 5, capro = 6, etc.), with a -lactone suffix and a Greek letter prefix that specifies the number of carbon atoms in the heterocycle — that is, the distance between the relevant -OH and the -COOH groups along said backbone.

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  9. Cheletropic reaction - Wikipedia

    en.wikipedia.org/wiki/Cheletropic_reaction

    In organic chemistry, cheletropic reactions, also known as chelotropic reactions, [2] are a type of pericyclic reaction (a chemical reaction that involves a transition state with a cyclic array of atoms and an associated cyclic array of interacting orbitals). [1] Specifically, cheletropic reactions are a subclass of cycloadditions.