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 |
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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: | 28 Aug 2021 20:26 |
URI: | http://eprints.hud.ac.uk/id/eprint/15460 |
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