Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4646
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Type: Journal article
Title: A cyclodextrin to reverse the regioselectivity of nitrile oxide cycloaddition to a terminal alkene
Author: Meyer, A.
Easton, C.
Lincoln, S.
Simpson, G.
Citation: Journal of the Chemical Society, Chemical Communications, 1997; 16(16):1517-1518
Publisher: ROYAL SOC CHEMISTRY
Issue Date: 1997
ISSN: 0022-4936
1364-548X
Abstract: The 1,3-dipolar cycloaddition of 4-tert-butylbenzonitrile oxide with 6A-acrylamido-6A-deoxy-β-cyclodextrin in aqueous solution favours formation of the 4-substituted isoxazoline, in contrast to the normal predominance of the 5-substituted regioisomer from reactions of monosubstituted alkenes.
DOI: 10.1039/a703575f
Published version: http://dx.doi.org/10.1039/a703575f
Appears in Collections:Aurora harvest 2
Chemistry publications
Environment Institute publications

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