Enantioselective Fluorescent Sensors for N-Boc-Protected Amino Acid Anions Based on BINOL
Author:
Publisher
Wiley
Subject
General Chemistry
Reference47 articles.
1. Enantioselective Recognition of Carboxylates: A Receptor Derived from α-Aminoxy Acids Functions as a Chiral Shift Reagent for Carboxylic Acids
2. A Highly Enantioselective Receptor for N-Protected Glutamate and Anomalous Solvent-Dependent Binding Properties
3. A novel chiral terpyridine macrocycle as a fluorescent sensor for enantioselective recognition of amino acid derivativesElectronic supplementary information (ESI) available: plots for estimation of binding constants for tpy macrocycle 1 with (R)-PhEtOMe. See http://www.rsc.org/suppdata/cc/b3/b313960c/
4. Colorimetric Sensors for Anion Recognition Based on the Proton Transfer Signaling Mechanism
5. New Macrocyclic Compound as Chiral Shift Reagent for Carboxylic Acids
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1. The Intramolecular Charge Transfer Mechanism by Which Chiral Self-Assembled H8-BINOL Vesicles Enantioselectively Recognize Amino Alcohols;International Journal of Molecular Sciences;2024-05-21
2. Recent advances of BINOL-based sensors for enantioselective fluorescence recognition;The Analyst;2020
3. Novel chiral Oxa-bridged Calix[2]arene[2]triazine derivatives as NMR chiral reagents for enantioselective recognition of α-racemic carboxylic acids;Journal of Inclusion Phenomena and Macrocyclic Chemistry;2019-04-27
4. Fluorescent Sensing of Chirality;Comprehensive Supramolecular Chemistry II;2017
5. (S)-BINOL Immobilized onto Multiwalled Carbon Nanotubes through Covalent Linkage: A New Approach for Hybrid Nanomaterials Characterization;ChemNanoMat;2015-04-13
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