Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4647
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Type: Journal article
Title: High enantioselectivity in the reactions of (R)- and (S)-1-phenylethylamine with 6A-deoxy-6A-iodo-β-cyclodextrin
Other Titles: High enantioselectivity in the reactions of (R)- and (S)-1-phenylethylamine with 6A-deoxy-6A-iodo-beta-cyclodextrin
Author: Easton, C.
Lincoln, S.
Schleibs, D.
Citation: Journal of the Chemical Society, Chemical Communications, 1995; 11(11):1167-1168
Publisher: The Society
Issue Date: 1995
ISSN: 0022-4936
Abstract: 6A-Deoxy-6A-iodo-β-cyclodextrin reacts with (R)-1-phenylethylamine one hundred and sixty times faster than it reacts with the corresponding (S)-enantiomer of the amine.
DOI: 10.1039/C39950001167
Published version: http://dx.doi.org/10.1039/c39950001167
Appears in Collections:Aurora harvest 2
Chemistry publications
Environment Institute publications

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