<sup>1</sup>H and<sup>2</sup>H nuclear magnetic resonance determination of the enantiomeric purity and absolute configuration of α-deuteriated primary carboxylic acids, alcohols, and amines
作者:David Parker
DOI:10.1039/p29830000083
日期:——
The enantiomericcomposition and absolute configuration of α-deuteriated primary carboxylic acids may be accurately determined by 1H and 2H nuclear magnetic resonance analysis of the corresponding esters of (S)-methyl 2-hydroxy-2-phenylethanoate (2). Similar methods with (S)-2-acetoxy-2-phenylethanoic acid (3) and (–)-camphanoyl chloride (1) as chiral reagents have enabled the enantiomeric purity of