A practical strategy to access chiral α-aryloxy carboxylic acids through ion-pairing directed asymmetric hydrogenation-Reference-Cited by-同舟云学术

A practical strategy to access chiral α-aryloxy carboxylic acids through ion-pairing directed asymmetric hydrogenation

Published:2020 Issue:24 Volume:7 Page:4069-4073
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Yao Lin¹²³⁴⁵^ORCID,Ma Haixia¹²³⁴⁵,Nie Zhuang⁶⁷⁸⁹¹⁰,Nie Huifang¹²³⁴⁵^ORCID,Zhang Dongxu¹²³⁴⁵,Wei Zhao¹²³⁴⁵,Shen Zhanhong¹²³⁴⁵,Chen Weiping¹²³⁴⁵^ORCID,Jiang Ru¹²³⁴⁵^ORCID,Zhang Shengyong¹²³⁴⁵

Affiliation:

1. Department of Medicinal Chemistry and Pharmaceutical Analysis

2. School of Pharmacy

3. Fourth Military Medical University

4. Xi'an

5. PR China

6. Key Laboratory of Resource Biology and Biotechnology in Western China

7. Ministry of Education

8. The College of Life Science

9. Northwest University

10. Xi'an 710069

Abstract

A series of optically active α-aryloxy functionalized carboxylic acids were obtained via non-covalent interaction assisted highly efficient asymmetric hydrogenation.

Funder

National Natural Science Foundation of China

Natural Science Basic Research Program of Shaanxi Province

Fourth Military Medical University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/QO/D0QO01205J

Reference26 articles.

1. Enhanced Activity of Single-Isomer Fenoxaprop on Cool-Season Grasses