Effective enantiomeric identification of aromatic amines by tyrosine-modified pillar[5]arenes as chiral NMR solvating agents-Reference-Cited by-同舟云学术

Effective enantiomeric identification of aromatic amines by tyrosine-modified pillar[5]arenes as chiral NMR solvating agents

Published:2021 Issue:15 Volume:8 Page:4144-4152
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Luzhi¹²³⁴⁵^ORCID,Ma Cuiguang¹²³⁴,He Qin¹²³⁴,Huang Yan⁶⁷⁴,Duan Wengui¹²³⁴

Affiliation:

1. School of Chemistry and Chemical Engineering

2. Guangxi University

3. Nanning 530004

4. P. R. China

5. Guangxi Key Laboratory of Electrochemical Energy Materials

6. Guangxi Institute of Chinese Traditional Medical & Pharmaceutical Science and Guangxi Key Laboratory of Traditional Chinese Medicine Quality Standards

7. Nanning 530022

Abstract

Two novel tyrosine-modified pillar[5]arenes have been synthesized and applied as chiral NMR solvating agents to establish an efficient ¹H NMR method for enantioselective recognition and configuration assignment towards α-aromatic ethylamines.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00525A

Reference71 articles.

1. Photo‐Controllable Catalysis and Chiral Monosaccharide Recognition Induced by Cyclodextrin Derivatives

2. Neutral Chiral Tetrakis‐Iodo‐Triazole Halogen‐Bond Donor for Chiral Recognition and Enantioselective Catalysis

3. Novel, Chiral, and Enantiopure C 2 ‐Symmetric Thioureas Promote Asymmetric Protio‐Pictet‐Spengler Reactions by Anion‐Binding Catalysis