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Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones

Moran, Wesley J. and Rodriguez, Arantxa (2012) Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones. Organic & Biomolecular Chemistry, 10 (43). pp. 8590-8592. ISSN 1477-0520

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    Abstract

    In the presence of an oxidant, sodium iodide is converted into hypoiodous acid which effects the rearrangement of tertiary propargylic alcohols to α-iodoenones in good yields.

    Item Type: Article
    Subjects: Q Science > Q Science (General)
    Q Science > QD Chemistry
    Schools: School of Applied Sciences
    Related URLs:
    Depositing User: Sara Taylor
    Date Deposited: 09 Oct 2012 10:18
    Last Modified: 26 Jul 2013 16:23
    URI: http://eprints.hud.ac.uk/id/eprint/15460

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