Chiral discrimination of secondary alcohols by both1H-NMR and HPLC after labeling with a chiral derivatization reagent, 2-(2,3-anthracenedicarboximide)cyclohexane carboxylic acid-Reference-Cited by-同舟云学术

Chiral discrimination of secondary alcohols by both1H-NMR and HPLC after labeling with a chiral derivatization reagent, 2-(2,3-anthracenedicarboximide)cyclohexane carboxylic acid

Published:2005 Issue:S1 Volume:17 Page:S171-S176
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Ohtaki Takashi,Akasaka Kazuaki,Kabuto Chizuko,Ohrui Hiroshi

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference18 articles.

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3. Determining factors in the assignment of the absolute configuration of alcohols by NMR. The use of anisotropic effects on remote positions;Seco;Tetrahedron,1997

4. On the use of the O-methylmandelate ester for establishment of absolute-configuration of secondary alcohols;Trost;J Org Chem,1986

5. 2-Methoxy-2-(1-naphthyl)propionic acid, a powerful chiral auxiliary for enantioresolution of alcohols and determination of their absolute configurations by the 1H NMR anisotropy method;Harada;Tetrahedron: Asymmetry,2000

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