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

Wesley J. Moran, Arantxa Rodríguez

Research output: Contribution to journalArticle

13 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.

LanguageEnglish
Pages8590-8592
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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Sodium Iodide
sodium iodides
Oxidants
alcohols
Alcohols
acids
hypoiodous acid

Cite this

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title = "Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones",
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.",
author = "Moran, {Wesley J.} and Arantxa Rodr{\'i}guez",
year = "2012",
month = "11",
day = "21",
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language = "English",
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journal = "Organic and Biomolecular Chemistry",
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publisher = "Royal Society of Chemistry",
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Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to α-iodoenones. / Moran, Wesley J.; Rodríguez, Arantxa.

In: Organic and Biomolecular Chemistry, Vol. 10, No. 43, 21.11.2012, p. 8590-8592.

Research output: Contribution to journalArticle

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AU - Moran, Wesley J.

AU - Rodríguez, Arantxa

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AB - 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.

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