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  2. Carbohydrate acetalisation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_acetalisation

    The latter reagent in itself is an acetal and therefore the reaction is actually a cross-acetalisation. Kinetic reaction control results from 2-methoxypropene as the reagent. D-ribose in itself is a hemiacetal and in equilibrium with the pyranose 3. In aqueous solution ribose is 75% pyranose and 25% furanose and a different acetal 4 is formed.

  3. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    In organic chemistry, a hemiacetal is a functional group the general formula R 1 R 2 C(OH)OR, where R 1, R 2 is a hydrogen atom or an organic substituent. They generally result from the nucleophilic addition of an alcohol (a compound with at least one hydroxy group ) to an aldehyde ( R−CH=O ) or a ketone ( R 2 C=O ) under acidic conditions.

  4. Category:Acetals - Wikipedia

    en.wikipedia.org/wiki/Category:Acetals

    Download as PDF; Printable version; ... Hemiacetals (1 C, 2 P) K. Ketals (1 C, 11 P) Pages in category "Acetals" The following 17 pages are in this category, out of ...

  5. Tetrahedral carbonyl addition compound - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_carbonyl...

    Acid catalyzed acetal formation from the corresponding hemiacetal. Acetals, as already pointed out, are stable tetrahedral intermediates so they can be used as protective groups in organic synthesis. Acetals are stable under basic conditions, so they can be used to protect ketones from a base. The acetal group is hydrolyzed under acidic conditions.

  6. Acetal - Wikipedia

    en.wikipedia.org/wiki/Acetal

    Acetals are stable compared to hemiacetals but their formation is a reversible equilibrium as with esters. As a reaction to create an acetal proceeds, water must be removed from the reaction mixture, for example, with a Dean–Stark apparatus , lest it hydrolyse the product back to the hemiacetal.

  7. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    Because of the greater stability of thioacetals, the equilibirum lies on the side of the acetal. In contradistinction to the O,O‑acetal case, it is not needed to remove water from the reaction mixture in order to shift the equilibrium. [65] S,O-Acetals are hydrolyzed a factor of 10,000 times faster than the corresponding S,S-acetals. Their ...

  8. Anomer - Wikipedia

    en.wikipedia.org/wiki/Anomer

    The anomeric centre in hemiacetals is the anomeric carbon C-1; in hemiketals, it is the carbon derived from the carbonyl of the ketone (e.g. C-2 in D-fructose). In aldohexoses the anomeric reference atom is the stereocenter that is farthest from the anomeric carbon in the ring (the configurational atom, defining the sugar as D or L ).

  9. Category:Hemiacetals - Wikipedia

    en.wikipedia.org/wiki/Category:Hemiacetals

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