Abstract
The absolute configurations of 2-methoxy-2-(1-naphthyl)propionic acid and 2-methoxy-2-(2-naphthyl)propionic acid were reconfirmed by NMR analyses of phenylglycine methyl ester (PGME) derivatives. Their absolute configurations determined by the PGME method are consistent with those obtained by the 1H NMR anisotropy method and X-ray crystallography.
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