Biological Sciences and Analytical Chemistry. Development of a new chiral derivatizing reagent, (+)-2-methyl-2-.BETA.-naphthyl-1,3-benzodioxole-4-carboxylic acid, for enantiomer analysis of amino acids.
Author:
Affiliation:
1. Department of Applied Biological Chemistry, Faculty of Agriculture, Tohoku University
Publisher
Japan Society for Analytical Chemistry
Subject
Analytical Chemistry
Link
http://www.jstage.jst.go.jp/article/bunsekikagaku1952/44/10/44_10_739/_pdf
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Recognition of the remote chiral center in lipase-catalyzed kinetic resolution of [2-methyl-2-(2′-naphthyl)-1,3-benzodioxol-4-yl]methyl acetate, the precursor of 2-methyl-2-(2′-naphthyl)-1,3-benzodioxole-4-carboxylic acid (MNB carboxylic acid);Journal of Molecular Catalysis B: Enzymatic;2014-11
2. Chemoenzymatic Synthesis of Both Enantiomers of 2-tert-Butyl-2-methyl-1,3-benzodioxole-4-carboxylic (TBMB) Acid;Advanced Synthesis & Catalysis;2010-09-24
3. Resolution of chiral drugs by liquid chromatography based upon diastereomer formation with chiral derivatization reagents;Journal of Biochemical and Biophysical Methods;2002-12
4. A Fluorometric Determination Method ford,lConfigurations of Per-O-Methylated Monosaccharides by Anomeric 2-Methyl-2-β-naphthyl-1,3-benzodioxole 4-Carboxylation and High-Performance Liquid Chromatography;Analytical Biochemistry;1997-03
5. Recent Progress in Liquid Chromatographic Enantioseparation Based upon Diastereomer Formation with Fluorescent Chiral Derivatization Reagents;Biomedical Chromatography;1996-11
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