A new approach for the determination of the absolute configuration of secondary alcohols by 1H NMR with O-substituted mandelate derivatives
✍ Scribed by Isabelle Chataigner; Jacques Lebreton; Didier Durand; André Guingant; Jean Villiéras
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 223 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
It is shown that the cheap and easily prepared mandelic acid esters (or their OAc analogues) are best suited than the expensive, although usually employed, OMe mandelic acid esters to assess both the enantiomeric excesses and absolute configurations of secondary alcohols.
📜 SIMILAR VOLUMES
## Abstract A novel methodology using a chiral molecular tool of MαNP acid (**1**), 2‐methoxy‐2‐(1‐naphthyl)propionic acid, useful for preparation of enantiopure secondary alcohols and determination of their absolute configurations by the ^1^H NMR anisotropy method was developed; racemic MαNP acid