p1,n1 salts: Self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid

The occurrence of p1,n1 salts can be exploited to sequester racemates; an application to technical mixtures of chrysanthemic acids (ChA) allowed the separation of trans- and cis-ChA and the recovery of the excess enantiomer of trans-ChA.

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Bibliographic Details
Published in:Chemical communications (Cambridge, England) England), 2006-11 (41), p.4294-4296
Main Authors: Rosini, Goffredo, Ayoub, Claudia, Borzatta, Valerio, Mazzanti, Andrea, Marotta, Emanuela, Righi, Paolo
Format: Article
Language:English
Online Access:Get full text
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Summary:The occurrence of p1,n1 salts can be exploited to sequester racemates; an application to technical mixtures of chrysanthemic acids (ChA) allowed the separation of trans- and cis-ChA and the recovery of the excess enantiomer of trans-ChA.
ISSN:1359-7345