Abstract
We report here a sensitive method for the determination of the absolute configurations of primary amines using exciton-coupled circular dichroism (ECCD). The method works on a microgram scale by derivatization of chiral amines with quinoline chromophores. Complexation of the chiral ligands with metal ion fixes the geometry of the chromophores, resulting in a twist that is governed by the asymmetric carbon configuration and steric environment of the amine. The absolute configurations of the primary amines can be interpreted from the couplets of the ECCD spectra of the derivatized complexes. Crystal structures, 2D NMR studies, and semiempirical calculations provide structural evidence for our model.
Original language | English (US) |
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Pages (from-to) | 180-189 |
Number of pages | 10 |
Journal | Chirality |
Volume | 15 |
Issue number | 2 |
DOIs | |
State | Published - 2003 |
Keywords
- Chiral primary amines
- Chirality
- Configurational assignment
- Exciton-coupled circular dichroism
- Metal complexation
ASJC Scopus subject areas
- Drug Discovery
- Analytical Chemistry
- Spectroscopy
- Catalysis
- Pharmacology
- Organic Chemistry