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V. Cyclization Reactions

  • Page ID
    24081
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    A radical generated from a Barton ester undergoes cyclization if it contains a properly positioned multiple bond (eq 1050).50,51 Such reactions are not common because unless the needed carboxylic acid is readily available, the steps involved in its synthesis often make this process less attractive than others for generating the carbohydrate radical needed for ring formation.

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    This page titled V. Cyclization Reactions is shared under a All Rights Reserved (used with permission) license and was authored, remixed, and/or curated by Roger W. Binkley and Edith R. Binkley.

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