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

Wesley J. Moran, Arantxa Rodríguez

Research output: Contribution to journalArticle

15 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)8590-8592
Number of pages3
JournalOrganic and Biomolecular Chemistry
Volume10
Issue number43
Early online date3 Oct 2012
DOIs
Publication statusPublished - 21 Nov 2012

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