Chiral Recognition Ability of an Optically Active Poly(diphenylacetylene) as a Chiral Stationary Phase for HPLC
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/advpub/0/advpub_160542/_pdf
Reference23 articles.
1. Optically active synthetic polymers as chiral stationary phases in HPLC
2. Efficient Separation of Enantiomers Using Stereoregular Chiral Polymers
3. Enantioseparation on Helical Poly(phenylacetylene)s Bearing Cinchona Alkaloid Pendants as Chiral Stationary Phases for HPLC
4. Synthesis of Helical Poly(phenylacetylene)s with Amide Linkage Bearing l-Phenylalanine and l-Phenylglycine Ethyl Ester Pendants and Their Applications as Chiral Stationary Phases for HPLC
5. Influence of stereoregularity and linkage groups on chiral recognition of poly(phenylacetylene) derivatives bearing L -leucine ethyl ester pendants as chiral stationary phases for HPLC
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1. Positive Synergy between the Helical Poly(phenylacetylene) Backbones and the Helical L-Proline Oligopeptide Pendants for Enhanced Enantioseparation Properties;Analytical Chemistry;2024-01-23
2. Facile Synthesis of Linear and Cyclic Poly(diphenylacetylene)s by Molybdenum and Tungsten Catalysis;Angewandte Chemie International Edition;2023-07-10
3. Facile Synthesis of Linear and Cyclic Poly(diphenylacetylene)s by Molybdenum and Tungsten Catalysis;Angewandte Chemie;2023-07-10
4. Thermally stable and rewritable circularly polarized luminescent helical poly(diphenylacetylene)s: stabilization of macromolecular helicity memory via reversible ion-pair formation;Journal of Materials Chemistry C;2023
5. Supramolecular chiral polymeric aggregates: Construction and applications;Aggregate;2022-09-06
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