Determination of the absolute configuration of linear secondary alcohols adopting one enantiomer of the chiral anisotropic reagents, methoxy-(1-and 2-naphthyl)acetic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
2. Are Both the (R)- and the (S)-MPA Esters Really Needed for the Assignment of the Absolute Configuration of Secondary Alcohols by NMR? The Use of a Single Derivative
3. Determination of the absolute configuration of yessotoxin, a polyether compound implicated in diarrhetic shellfish poisoning, by NMR spectroscopic method using a chiral anisotropic reagent, methoxy-(2-naphthyl)acetic acid
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3. Chiral Molecular Tools Powerful for the Preparation of Enantiopure Compounds and Unambiguous Determination of Their Absolute Configurations by X-Ray Crystallography and/or 1H NMR Diamagnetic Anisotropy;Chiral Analysis;2018
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