Organic Chemistry Frontiers, volume 8, issue 15, pages 4144-4152

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

Luzhi Liu ^{1, 2}

Cuiguang Ma ¹

Qin He ¹

Yan Huang ³

Wengui Duan ¹

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School of Chemistry and Chemical Engineering, Guangxi University, Nanning 530004, Guangxi, P. R. China |

Guangxi Key Laboratory of Electrochemical Energy Materials, Nanning, Guangxi 530004, P. R. China |

Guangxi Institute of Chinese Traditional Medical & Pharmaceutical Science and Guangxi Key Laboratory of Traditional Chinese Medicine Quality Standards, Nanning 530022, Guangxi, P. R. China |

Publication type: Journal Article

Publication date: 2021-05-27

Royal Society of Chemistry (RSC)

Journal: Organic Chemistry Frontiers

scimago Q1

SJR: 1.016

CiteScore: 7.8

Impact factor: 4.6

ISSN: 20524110, 20524129

DOI: 10.1039/d1qo00525a

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Organic Chemistry

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.

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Publisher

Royal Society of Chemistry (RSC)

Journal

Organic Chemistry Frontiers

scimago Q1

SJR

1.016

CiteScore

7.8

Impact factor

4.6

ISSN

20524110 (Print)

20524129 (Electronic)

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

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