Determination of the absolute configuration of linear secondary alcohols adopting one enantiomer of the chiral anisotropic reagents, methoxy-(1-and 2-naphthyl)acetic acids
- 29 October 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (44) , 8113-8116
- https://doi.org/10.1016/s0040-4039(98)01800-0
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- 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 DerivativeJournal of the American Chemical Society, 1998
- 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 acidTetrahedron Letters, 1996
- High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoidsJournal of the American Chemical Society, 1991