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.
G. Rosini, C. Ayoub, V. Borzatta, A. Mazzanti, E. Marotta, P. Righi (2006). p1,n1 Salts: self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid. CHEMICAL COMMUNICATIONS, 2006, 4294-4296 [10.1039/b608405b].
p1,n1 Salts: self-assembled supramolecular structures sequestering racemates. Diastereomeric separation and enantiomeric enrichment of trans-chrysanthemic acid
ROSINI, GOFFREDO;MAZZANTI, ANDREA;MAROTTA, EMANUELA;RIGHI, PAOLO
2006
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.File in questo prodotto:
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