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Literature DB >> 15367983

A highly congested N,N'-dioxide fluorosensor for enantioselective recognition of chiral hydrogen bond donors.

Abstract

A rigid C2-symmetric 1,8-diacridylnaphthalene N,N'-dioxide fluorosensor has been developed for enantioselective recognition of chiral hydrogen bond donors such as amines and amino acids. Copyright 2004 The Royal Society of Chemistry

Entities: Chemical

Year: 2004 PMID： 15367983 DOI： 10.1039/b407718k

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

10 in total

1. Enantioselective fluorescent sensors for amino acid derivatives based on BINOL bearing S-tryptophan unit: synthesis and chiral recognition.

Authors: Kuo-Xi Xu; Peng-Fei Cheng; Jin Zhao; Chao-Jie Wang
Journal: J Fluoresc Date: 2010-01-07 Impact factor: 2.217

2. Regioselective copper-catalyzed amination of bromobenzoic acids using aliphatic and aromatic amines.

Authors: Christian Wolf; Shuanglong Liu; Xuefeng Mei; Adam T August; Michael D Casimir
Journal: J Org Chem Date: 2006-04-14 Impact factor: 4.354

3. Regioselective copper-catalyzed amination of chlorobenzoic acids: synthesis and solid-state structures of N-aryl anthranilic acid derivatives.

Authors: Xuefeng Mei; Adam T August; Christian Wolf
Journal: J Org Chem Date: 2006-01-06 Impact factor: 4.354

4. Regioselective Copper-catalyzed C-N and C-S Bond Formation using Amines, Thiols and Halobenzoic Acids.

Authors: Shuanglong Liu; John Paul C Pestano; Christian Wolf
Journal: Synthesis (Stuttg) Date: 2007-11-16 Impact factor: 3.157

5. Enantioselective Recognition of Chiral Carboxylic Acids by a β-Amino Acid and 1,10-Phenanthroline Based Chiral Fluorescent Sensor.

Authors: Yonghong Zhang; Fangzhi Hu; Bin Wang; Xiaomei Zhang; Chenjiang Liu
Journal: Sensors (Basel) Date: 2015-05-06 Impact factor: 3.576

10. Optically Pure Aziridin-2-yl Methanols as Readily Available ¹H NMR Sensors for Enantiodiscrimination of α-Racemic Carboxylic Acids Containing Tertiary or Quaternary Stereogenic Centers.

Authors: Martyna Malinowska; Szymon Jarzyński; Adam Pieczonka; Michał Rachwalski; Stanisław Leśniak; Anna Zawisza
Journal: J Org Chem Date: 2020-09-02 Impact factor: 4.354

10 in total

A highly congested N,N'-dioxide fluorosensor for enantioselective recognition of chiral hydrogen bond donors.

1. Enantioselective fluorescent sensors for amino acid derivatives based on BINOL bearing S-tryptophan unit: synthesis and chiral recognition.

2. Regioselective copper-catalyzed amination of bromobenzoic acids using aliphatic and aromatic amines.

3. Regioselective copper-catalyzed amination of chlorobenzoic acids: synthesis and solid-state structures of N-aryl anthranilic acid derivatives.

4. Regioselective Copper-catalyzed C-N and C-S Bond Formation using Amines, Thiols and Halobenzoic Acids.

5. Enantioselective Recognition of Chiral Carboxylic Acids by a β-Amino Acid and 1,10-Phenanthroline Based Chiral Fluorescent Sensor.

6. Chiral ¹H NMR of Atropisomeric Quinazolinones With Enantiopure Phosphoric Acids.

7. Chiral Phosphoric Acid Promoted Chiral 1H NMR Analysis of Atropisomeric Quinolines.

8. Determination of enantiomeric excess of carboxylates by fluorescent macrocyclic sensors.

9. Synthesis and Evaluation of the (S)-BINAM Derivatives as Fluorescent Enantioselective Detectors.

10. Optically Pure Aziridin-2-yl Methanols as Readily Available ¹H NMR Sensors for Enantiodiscrimination of α-Racemic Carboxylic Acids Containing Tertiary or Quaternary Stereogenic Centers.