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

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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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Official URL: http://dx.doi.org/10.1039/C2OB26360B

DOI: 10.1039/C2OB26360B

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:	Author
Depositing User:	Sara Taylor
Date Deposited:	09 Oct 2012 10:18
Last Modified:	25 Oct 2012 09:28
URI:	http://eprints.hud.ac.uk/id/eprint/15460

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