Use of shift reagent with mtpa derivatives in 19F NMR spectroscopy: III. Determination of absolute configuration and enantiomeric purity of secondary alcohols
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19780870707/fullpdf
Reference12 articles.
1. Use of Shift Reagent with MTPA Derivatives in 19F NMR Spectroscopy: Determination of Absolute Configuration of Stereomeric 2- and 3- Substituted Cyclohexanols
2. E. M. Merckx A. J. van de Wal Tijdingen van de Vlaamse Chemische Vereniging 1978
3. Use of shift reagent with diastereomeric MTPA esters for determination of configuration and enantiomeric purity of secondary carbinols in 1H NMR spectroscopy
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1. Enzymatic “in Vitro” Reduction of Ketones: Part 9. Preparation of Pure (1S, 2S)-2-Chlorocyclohexanol;Bulletin des Sociétés Chimiques Belges;2010-09-01
2. Enzymatic “in vitro” reduction of ketones. IV. (1) Preparative scale reductions of cyclohexanone derivatives in an ethanol-NAD+-HLAD system.;Bulletin des Sociétés Chimiques Belges;2010-09-01
3. Enzymatic In Vitro Reduction of Ketones. Part 111. The Unexpected Steric Course of the HLAD Catalyzed Reduction of 3-Cyanocyclohexanone;Bulletin des Sociétés Chimiques Belges;2010-09-01
4. A correlation of configuration and19F-NMR Chemical Shifts of (R)-(+)-Mosher Esters of Chiral Cyclopentanediol Derivatives;Journal f�r Praktische Chemie/Chemiker-Zeitung;1992
5. Determination of the absolute configuration and enantiomeric purity of alcohols from the13C-NMR spectra of the corresponding MTPA esters;Chirality;1990
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