Reliable assignment of absolute configuration of chiral amines based on the analysis of 1H NMR spectra of their CFTA amide diastereomers-Reference-Cited by-同舟云学术

Reliable assignment of absolute configuration of chiral amines based on the analysis of 1H NMR spectra of their CFTA amide diastereomers

Published:2008-04 Issue:7 Volume:19 Page:847-856
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Fujiwara Tomoya,Segawa Masaru,Fujisawa Hidehito,Murai Taiki,Takahashi Tamiko,Omata Kenji,Kabuto Kuninobu,Lodwig Siegfried N.,Unkefer Clifford J.,Takeuchi Yoshio

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference23 articles.

1. The Assignment of Absolute Configuration by NMR

2. Chiral reagents for the determination of enantiomeric excess and absolute configuration using NMR spectroscopy

3. .alpha.-Methoxy-.alpha.-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines

4. Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters

5. Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivatives

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