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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/16836

Title: Isoxazole to oxazole: a mild and unexpected transformation
Authors: Jones, Raymond C.F.
Chatterley, Alexander
Marty, Romain
Owton, W. Martin
Elsegood, Mark R.J.
Issue Date: 2015
Publisher: Royal Society of Chemistry
Citation: JONES, R.C.F. ... et al., 2015. Isoxazole to oxazole: a mild and unexpected transformation. Chemical Communications, 51 (6), pp. 1112 - 1115.
Abstract: 3-Aryltetrahydrobenzisoxazoles prepared en route to the coleophomone natural products and analogues, were found to undergo a remarkable base-mediated rearrangement to 2-aryltetrahydrobenzoxazoles. The scope of this unprecedented, facile transformation was probed: a range of analogues was produced, a mechanism proposed, and an application demonstrated by synthesis of a known herbicidal compound.
Description: This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Version: Published
DOI: 10.1039/c4cc07999j
URI: https://dspace.lboro.ac.uk/2134/16836
Publisher Link: http://dx.doi.org/10.1039/c4cc07999j
ISSN: 1359-7345
Appears in Collections:Published Articles (Chemistry)

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