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  2. Carbohydrate acetalisation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_acetalisation

    In carbohydrate chemistry carbohydrate acetalisation is an organic reaction and a very effective means of providing a protecting group. The example below depicts the acetalisation reaction of D-ribose 1. With acetone or 2,2-dimethoxypropane as the acetalisation reagent the reaction is under thermodynamic reaction control and results in the ...

  3. Protecting group - Wikipedia

    en.wikipedia.org/wiki/Protecting_group

    Photolabile protecting groups bear a chromophore, which is activated through radiation with an appropriate wavelength and so can be removed. [6] For examples the o-nitrobenzylgroup ought be listed here. The rare double-layer protecting group is a protected protecting group, which exemplify high stability.

  4. Acetal - Wikipedia

    en.wikipedia.org/wiki/Acetal

    Used in a more general sense, the term X,Y-acetal also refers to any functional group that consists of a carbon bearing two heteroatoms X and Y. For example, N,O-acetal refers to compounds of type R 1 R 2 C(OR)(NR' 2) (R,R' ≠ H) also known as a hemiaminal ether or Aminal, a.k.a. aminoacetal.

  5. Armed and disarmed saccharides - Wikipedia

    en.wikipedia.org/wiki/Armed_and_disarmed_saccharides

    These protecting groups “lock” the sugars into a rigid chair conformation. When the sugar forms the necessary oxocarbenium ion, it flattens at the anomeric position. This change in configuration is a high-energy transformation when cyclic protecting groups are present, and leads to the sugar being “disarmed”. [3] These groups can be ...

  6. Acetonide - Wikipedia

    en.wikipedia.org/wiki/Acetonide

    In organic chemistry, an acetonide is the functional group composed of the cyclic ketal of a diol with acetone. The more systematic name for this structure is an isopropylidene ketal. Acetonide is a common protecting group for 1,2- and 1,3-diols. [1] The protecting group can be removed by hydrolysis of the ketal using dilute aqueous acid.

  7. Category:Protecting groups - Wikipedia

    en.wikipedia.org/wiki/Category:Protecting_groups

    Cyclic acetals (8 C) Pages in category "Protecting groups" The following 19 pages are in this category, out of 19 total. This list may not reflect recent changes. ...

  8. Benzylidene compounds - Wikipedia

    en.wikipedia.org/wiki/Benzylidene_compounds

    Benzylidene acetal is a protecting group in synthetic organic chemistry of the form PhCH(OR) 2. For example, 4,6-O-benzylidene-glucopyranose is a glucose derivative. Benzylidene is an archaic term for compounds of the type PhCHX 2 and PhCH= substituents (Ph = C 6 H 5). For example, dibenzylideneacetone is (PhCH=CH) 2 CO.

  9. Benzylidene acetal - Wikipedia

    en.wikipedia.org/wiki/Benzylidene_acetal

    Structure of the benzylidene acetal of glucose. In organic chemistry , a benzylidene acetal is the functional group with the structural formula C 6 H 5 CH(OR) 2 (R = alkyl, aryl). Benzylidene acetals are used as protecting groups in glycochemistry.