Use of Axially Chiral 2′-Methoxy-1,1′-binaphthyl-2-carboxylic Acid as Chiral Derivatizing Agent for Discrimination of Enantiomeric Alcohols and Amines by1H NMR
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/62/12/62_12_3886/_pdf
Reference17 articles.
1. Optical Resolution of 2′-Methoxy-1,1′-binaphthyl-2-carboxylic Acid, and Application to Chiral Derivatizing Agent for HPLC Separation of Enantiomeric Alcohols and Amines
2. Use of shift reagent with diastereomeric MTPA esters for determination of configuration and enantiomeric purity of secondary carbinols in 1H NMR spectroscopy
3. Determination of absolute configuration and enantiomeric purity of spirocyclic alcohols by 1h nmr
4. .alpha.-Methoxy-.alpha.-(trifluoromethyl)benzyl isocyanate. A convenient reagent for the determination of the enantiomeric composition of primary and secondary amines
5. Syntheses of New Optically Active Organosilanes and Their Applications for the Optical-Purity-Determining Agents
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2. REFERENCES;Differentiation of Chiral Compounds Using NMR Spectroscopy;2018-06-15
3. Configurational Assignment of ‘Cryptochiral’ 10-Hydroxystearic Acid Through an Asymmetric Catalytic Synthesis;Helvetica Chimica Acta;2016-11-09
4. Enantioselective Synthesis of Axially Chiral Hydroxy Carboxylic Acid Derivatives by Rhodium-Catalyzed [2 + 2 + 2] Cycloaddition;The Journal of Organic Chemistry;2011-02-16
5. Resolution of inherently chiral anti-O,O′-dialkylated calix[4]arenes and determination of their absolute stereochemistries by CD and X-ray methods;Tetrahedron: Asymmetry;2005-02
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