Direct 1H NMR assay of the enantiomeric composition of amines and β-amino alcohols using o-acetyl mandelic acid as a chiral solvating agent
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines
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3. 2-Chloro-4(R),5(R)-dimethyl-2-oxo-1,3,2-dioxaphospholane, a new chiral derivatizing agent
4. 1H and2H nuclear magnetic resonance determination of the enantiomeric purity and absolute configuration of α-deuteriated primary carboxylic acids, alcohols, and amines
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1. A Chemoenzymatic Process to Achieve Optically Active Mandelic Acid Employing Continuous-Flow Resolution of Cyanohydrin as a Key Step;Revista Virtual de Química;2023
2. Enantioselective Recognition of Racemic Amino Alcohols in Aqueous Solution by Chiral Metal‐Oxide Keplerate {Mo 132 } Cluster Capsules;Chemistry – A European Journal;2021-07-30
3. Comparison of chiral NMR solvating agents for the enantiodifferentiation of amines;Tetrahedron;2018-09
4. REFERENCES;Differentiation of Chiral Compounds Using NMR Spectroscopy;2018-06-15
5. (+)-BINOL and Pure Shift Experiment: A Bidirectional Approach for NMR Chiral Discrimination of Overcrowded Spectra of Primary Amines;Journal of the Brazilian Chemical Society;2018
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