Issue 11, 1995
From the journal:

Journal of the Chemical Society, Chemical Communications

High enantioselectivity in the reactions of (R)- and (S)-1-phenylethylamine with 6A-deoxy-6A-iodo-β-cyclodextrin

Christopher J. Easton,   Stephen F. Lincoln  and  Darren M. Schliebs  

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.

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Article information

DOI
https://doi.org/10.1039/C39950001167
Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 1167-1168

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High enantioselectivity in the reactions of (R)- and (S)-1-phenylethylamine with 6A-deoxy-6A-iodo-β-cyclodextrin

C. J. Easton, S. F. Lincoln and D. M. Schliebs, J. Chem. Soc., Chem. Commun., 1995, 1167 DOI: 10.1039/C39950001167

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