221. A.-S. Chauvin, G. Bernardinelli, A. Alexakis,
     “Determination of the absolute configuration of chiral cyclic alcohols using diamine derivatizing agents by ³¹P NMR spectroscopy”
     Tetrahedron: Asymmetry 2006, 17, 2203-2209.

The absolute configuration and enantiomeric excess of chiral cyclic alcohols can be predicted from the ³¹P NMR spectra of the two diastereoisomers obtained with organophosphorus diamino-derivatizing agents (CDAs) and the chiral secondary alcohol, according to a simplified model taking into account the spatial location of the substituents of the chiral alcohol center and the ³¹P NMR signals of the two diastereoisomers.

DOI : 10.1016/j.tetasy.2006.07.042 

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