S-(+)-1-Methyl-2-(2,3-naphthalimido)ethyl Trifluoromethanesulfonate as a Fluorescence Chiral Labeling Reagent for Carboxylic Acid Enantiomers.-Reference-Cited by-同舟云学术

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S-(+)-1-Methyl-2-(2,3-naphthalimido)ethyl Trifluoromethanesulfonate as a Fluorescence Chiral Labeling Reagent for Carboxylic Acid Enantiomers.

Published:1995 Issue:2 Volume:11 Page:295-297
ISSN:0910-6340
Container-title:Analytical Sciences
language:en
Short-container-title:Anal. Sci.

Author:

YASAKA Yuta¹,MATSUMOTO Takashi¹,TANAKA Minoru¹

Affiliation:

1. Research Center for Environmental Preservation, Osaka University

Publisher

Springer Science and Business Media LLC

Subject

Analytical Chemistry

Link

http://www.jstage.jst.go.jp/article/analsci1985/11/2/11_2_295/_pdf

Cited by 16 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. High-Performance Liquid Chromatographic Enantioseparation Based on Diastereomer Formation with New Fluorescent Chiral Quinoxalines;HETEROCYCLES;2005

2. Synthesis of Azine-type Heterocyclic Compounds and Their Conversion into Functional Molecules;Journal of Synthetic Organic Chemistry, Japan;2004

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. Fluorescent tagging of physiologically important carboxylic acids, including fatty acids, for their detection in liquid chromatography;Analytica Chimica Acta;2002-08

5. Selectivity enhancement of diastereomer separation in RPLC using crystalline-organic phase-bonded silica;Chromatographia;2002-07

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