Published in

Royal Society of Chemistry, New Journal of Chemistry, 1(31), p. 86-92

DOI: 10.1039/b610587d

Links

Tools

Export citation

Search in Google Scholar

Discrimination of the enantiomers of new biphenylic derivatives in chiral micellar aggregates

Journal article published in 2007 by Francesca Ceccacci ORCID, Luisa Giansanti, Giovanna Mancini, Paolo Mencarelli, Alessandro Sorrenti
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Upload
Orange circle
Postprint: archiving restricted
Upload
Red circle
Published version: archiving forbidden
Policy details
Data provided by SHERPA/RoMEO

Abstract

The synthesis and characterization of two new chiral biphenylic derivatives is reported. The rotational barriers have been calculated on simpler homologues. The racemic mixtures of the two compounds have been used as probes of chirality for exploring the sites of chiral recognition in chiral micellar aggregates. Results suggest that one of the sites of chiral discrimination is the hydrophobic part of the aggregates, far from the stereogenic centres.