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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 09:18
Last Modified: 26 Jul 2013 15:23
URI: http://eprints.hud.ac.uk/id/eprint/15460

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