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The orientation of a tertiary amide group adjacent to an aromatic ring may be governed by the stereochemistry of an adjacent chiral substituent. With a chiral substituent in both ortho positions, matched/mismatched pairs of isomers result. Evidence for matched stereochemistry is provided by the clean NMR spectra of single conformers, while mismatching gives poor or unexpected selectivities in the formation of chiral substituents, or mixtures of amide conformers. Attempts to use the match-mismatch effect to select for racemic pairs of enantiomeric substituents, and hence develop a "racemate-sequestering" reagent, are described, along with the use of "matching" to scavenge a single enantiomer of a diamine from material of incomplete enantiomeric purity.

Original publication

DOI

10.1039/b514558a

Type

Journal article

Journal

Org Biomol Chem

Publication Date

07/02/2006

Volume

4

Pages

444 - 454

Keywords

Aldehydes, Amines, Benzamides, Crystallography, X-Ray, Ephedrine, Imidazolines, Magnetic Resonance Spectroscopy, Molecular Conformation, Oxazoles, Proline, Safrole, Stereoisomerism, Trimethylsilyl Compounds