Discrimination of enantiomers of amides with two stereogenic centers enabled by chiral bisthiourea derivatives using 1H NMR spectroscopy-Reference-Cited by-同舟云学术

Discrimination of enantiomers of amides with two stereogenic centers enabled by chiral bisthiourea derivatives using 1H NMR spectroscopy

Published:2021 Issue:30 Volume:19 Page:6697-6706
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhang Hanchang¹²³⁴,Zhao Hongmei⁵⁶⁷⁸⁴,Wen Jie¹²³⁴,Zhang Zhanbin¹²³⁴,Stavropoulos Pericles⁹¹⁰¹¹¹²,Li Yanlin¹²³⁴,Ai Lin¹²³⁴^ORCID,Zhang Jiaxin¹²³⁴

Affiliation:

1. College of Chemistry

2. Beijing Normal University

3. Beijing 100875

4. P. R. China

5. State Key Laboratory of Information Photonics and Optical Communications

6. School of Science

7. Beijing University of Posts and Telecommunications

8. Beijing 100876

9. Department of Chemistry

10. Missouri University of Science and Technology

11. Rolla

12. USA

Abstract

Enantiomers of amides with two stereogenic centers have been effectively discriminated in the presence of chiral bisthiourea derivatives as chiral solvating agents by ¹H NMR spectroscopy.

Funder

Beijing Normal University

National Institutes of Health

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB00742D

Reference59 articles.

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5. Immobilized Cellulose-Based Chiralpak IC Chiral Stationary Phase for Enantioseparation of Eight Imidazole Antifungal Drugs in Normal-Phase, Polar Organic Phase and Reversed-Phase Conditions Using High-Performance Liquid Chromatography

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