Literature DB >> 26479579

(1)H NMR chiral analysis of charged molecules via ion pairing with aluminum complexes.

Min-Seob Seo1, Hyunwoo Kim1,2.   

Abstract

Chiral analysis, such as determination of identity, concentration, and relative ratio of optically active (chiral) molecules, plays an indispensable role in contemporary synthetic, medicinal, and biological chemistry. Here, we describe the selective control of metal-centered chirality in an octahedral geometry to prepare negatively charged Al(III) complexes, which can be used as versatile (1)H NMR chiral solvating agents for both positively and negatively charged chiral molecules in polar or nonpolar solvents. During the formation of ion pairs between the Al(III) complexes and the chiral analytes such as amines and carboxylic acids, the metal-centered chirality in the Al complexes plays a crucial role in providing anisochronous chemical shifts to the (1)H NMR spectra. As a chiral solvating agent, Al(III) complexes display an unprecedentedly broad substrate scope, good solvent compatibility, and operational simplicity.

Entities:  

Year:  2015        PMID: 26479579     DOI: 10.1021/jacs.5b09555

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  13 in total

1.  Discrimination of Enantiomers of Dipeptide Derivatives with Two Chiral Centers by Tetraaza Macrocyclic Chiral Solvating Agents Using 1H NMR Spectroscopy.

Authors:  Lixia Fang; Caixia Lv; Guo Wang; Lei Feng; Pericles Stavropoulos; Guangpeng Gao; Lin Ai; Jiaxin Zhang
Journal:  Org Chem Front       Date:  2016-09-30       Impact factor: 5.281

2.  Chiral discrimination of α-hydroxy acids and N-Ts-α-amino acids induced by tetraaza macrocyclic chiral solvating agents by using 1H NMR spectroscopy.

Authors:  Caixia Lv; Lei Feng; Hongmei Zhao; Guo Wang; Pericles Stavropoulos; Lin Ai
Journal:  Org Biomol Chem       Date:  2017-01-27       Impact factor: 3.876

3.  Chiral Recognition of Hydantoin Derivatives Enabled by Tetraaza Macrocyclic Chiral Solvating Agents Using 1H NMR Spectroscopy.

Authors:  Jie Wen; Lei Feng; Hongmei Zhao; Li Zheng; Pericles Stavropoulos; Lin Ai; Jiaxin Zhang
Journal:  J Org Chem       Date:  2022-06-08       Impact factor: 4.198

4.  Synthesis of Tripeptide Derivatives with Three Stereogenic Centers and Chiral Recognition Probed by Tetraaza Macrocyclic Chiral Solvating Agents Derived from d-Phenylalanine and (1 S,2 S)-(+)-1,2-Diaminocyclohexane via 1H NMR Spectroscopy.

Authors:  Lei Feng; Guangpeng Gao; Hongmei Zhao; Li Zheng; Yu Wang; Pericles Stavropoulos; Lin Ai; Jiaxin Zhang
Journal:  J Org Chem       Date:  2018-10-30       Impact factor: 4.354

Review 5.  Recent Advances in Multinuclear NMR Spectroscopy for Chiral Recognition of Organic Compounds.

Authors:  Márcio S Silva
Journal:  Molecules       Date:  2017-02-07       Impact factor: 4.411

6.  Racemic vs. enantiopure inert Ti(iv) complex of a single diaminotetrakis(phenolato) ligand in anticancer activity toward human drug-sensitive and -resistant cancer cell lines.

Authors:  Maya Miller; Edit Y Tshuva
Journal:  RSC Adv       Date:  2018-11-27       Impact factor: 4.036

7.  A Gallium-based Chiral Solvating Agent Enables the Use of 1H NMR Spectroscopy to Differentiate Chiral Alcohols.

Authors:  Sumin Jang; Hyunwoo Kim
Journal:  iScience       Date:  2019-08-02

8.  Enantioselective Bifunctional Ammonium Salt-Catalyzed Syntheses of 3-CF3S-, 3-RS-, and 3-F-Substituted Isoindolinones.

Authors:  Andreas Eitzinger; Jan Otevrel; Victoria Haider; Antonio Macchia; Antonio Massa; Kirill Faust; Bernhard Spingler; Albrecht Berkessel; Mario Waser
Journal:  Adv Synth Catal       Date:  2021-02-17       Impact factor: 5.837

9.  The robust, readily available cobalt(iii) trication [Co(NH2CHPhCHPhNH2)3]3+ is a progenitor of broadly applicable chirality and prochirality sensing agents.

Authors:  Quang H Luu; Kyle G Lewis; Anik Banerjee; Nattamai Bhuvanesh; John A Gladysz
Journal:  Chem Sci       Date:  2018-05-11       Impact factor: 9.825

10.  Pd-Catalyzed Allylation of Imines to Access α-CF3-Substituted α-Amino Acid Derivatives.

Authors:  Michael Winter; Hyunwoo Kim; Mario Waser
Journal:  European J Org Chem       Date:  2019-10-09
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