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Carbonyl Protecting Groups

  • Page ID
    23476
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    Acetals and Ketals

    Cyclic acetals and ketals are the most useful carbonyl (aldehyde or ketone) protecting groups. Common diols used to form ketals are show below in order of their relative rate of formation.

    CO-diols.png

    1,3-dioxanes cleave faster than 1,3-dioxolanes.

    CO-cleavagerate1.png

    Acetals and ketals are easily formed and cleaved.

    CO-Ketals.png

    In general, saturated ketones can be selectively protected in the presence of a,b-unsaturated ketones

    CO-selective.png

    See: J. Org. Chem., 1986, 51, 773-784.

    Conditions have also been developed to reverse this selectivity:

    CO-revSelective.png

    See: Tetrahedron Lett., 1980, 21, 1357-1358.

    Carboxylic Acid Protecting Groups

    Esters

    Ester protecting groups are analogous to the carbamate protecting groups used to protect amines.

    Orthoesters

    COOH-OBO.png

    Contributors

    • Stephen Laws


    Carbonyl Protecting Groups is shared under a CC BY-NC-SA 4.0 license and was authored, remixed, and/or curated by LibreTexts.

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