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

Literature Information

Publication Date 2006-08-21
DOI 10.1039/B608405B
Impact Factor 6.222
Authors

Goffredo Rosini, Claudia Ayoub, Valerio Borzatta, Andrea Mazzanti, Emanuela Marotta, Paolo Righi


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Abstract

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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