Issue 68, 2012

Enhanced enantioselectivity of 3-methylcyclohexanone by mixed diol host compounds

Abstract

3-Methylcyclohexanone is only partially resolved by crystallisation with a chiral diol host compound (ee 40%), but when recrystallised from an equimolar mixture of the chiral diol host and a similar but achiral host we obtain complete resolution. The latter host acts as a nucleation inhibitor and the enhanced resolution is attributed to kinetic effects.

Graphical abstract: Enhanced enantioselectivity of 3-methylcyclohexanone by mixed diol host compounds

Supplementary files

Article information

Article type
Communication
Submitted
08 Jun 2012
Accepted
29 Jun 2012
First published
04 Jul 2012

Chem. Commun., 2012,48, 8526-8528

Enhanced enantioselectivity of 3-methylcyclohexanone by mixed diol host compounds

L. R. Nassimbeni, H. Su and T. Curtin, Chem. Commun., 2012, 48, 8526 DOI: 10.1039/C2CC34118B

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