A very mild and selective method for O-benzoylation of hydroxamic acids

    Authors

    Y. S. Zheng; M. Q. Liu;Y. Yuan

    Comments

    Authors: contact us about adding a copy of your work at [email protected]

    Abbreviated Journal Title

    Tetrahedron Lett.

    Keywords

    Benzoylation; Hydroxamic acid; Benzoyl peroxide; Nucleophilic attack; INTRAMOLECULAR AMINOHYDROXYLATION; BORONIC ACIDS; OXIDANT; Chemistry, Organic

    Abstract

    Selective O-benzoylation of hydroxamic acids is achieved by the alcohols are not reactive under these conditions. Various radical are compatible with this protocol, and no anhydrous reagents or of the benzoylations. treatment of BPO and DABCO. Aliphatic or oxidation sensitive functional groups solvents are required for the high yields (C) 2014 Elsevier Ltd. All rights reserved.

    Journal Title

    Tetrahedron Letters

    Volume

    55

    Issue/Number

    31

    Publication Date

    1-1-2014

    Document Type

    Article

    Language

    English

    First Page

    4404

    Last Page

    4406

    WOS Identifier

    WOS:000339695700028

    ISSN

    0040-4039

    Share

    COinS
     

    Accessibility Statement

    This item was created or digitized prior to April 24, 2027, or is a reproduction of legacy media created before that date. It is preserved in its original, unmodified state specifically for research, reference, or historical recordkeeping. In accordance with the ADA Title II Final Rule, the University Libraries provides accessible versions of archival materials upon request. To request an accommodation for this item, please submit an accessibility request form.