Issue 10, 1992
From the journal:

Journal of the Chemical Society, Chemical Communications

New chiral selectors derived from lactic acid. Cocrystalline and sorptive optical resolutions, and the crystal structure of an inclusion complex with 3-methylcyclohexanone

Edwin Weber,   Claus Wimmer,   Antonio L. Llamas-Saiz  and  Concepcion Foces-Foces  

Abstract

A new type of optically active clathrate formers derived from lactic acid, 1, is described, enabling useful enantiomer separations of different chiral compounds via cocrystallization and, for the first time, via sorption; the X-ray structure of the 2:1 inclusion complex between 1a and 3-methylcyclohexanone is reported.

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Article information

DOI
https://doi.org/10.1039/C39920000733
Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 733-735

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New chiral selectors derived from lactic acid. Cocrystalline and sorptive optical resolutions, and the crystal structure of an inclusion complex with 3-methylcyclohexanone

E. Weber, C. Wimmer, A. L. Llamas-Saiz and C. Foces-Foces, J. Chem. Soc., Chem. Commun., 1992, 733 DOI: 10.1039/C39920000733

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