An<scp>l</scp>-proline-modified chiral porous hyper-crosslinked<scp>l</scp>-phenylalanine dipeptide—increased reaction rate and selectivity in asymmetric catalysis-Reference-Cited by-同舟云学术

Anl-proline-modified chiral porous hyper-crosslinkedl-phenylalanine dipeptide—increased reaction rate and selectivity in asymmetric catalysis

Published:2023 Issue:10 Volume:14 Page:1124-1134
ISSN:1759-9954
Container-title:Polymer Chemistry
language:en
Short-container-title:Polym. Chem.

Author:

Wang Yaodong¹,Liu Lijia¹²^ORCID,Wang Yudan¹^ORCID,Sang Kexiao¹,Zhang Chunhong¹²^ORCID,Satoh Toshifumi³^ORCID

Affiliation:

1. Key Laboratory of Superlight Materials & Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin, 150001, China

2. Yantai Research Institute of Harbin Engineering University, Yantai, 264006, China

3. Faculty of Engineering, Hokkaido University, Sapporo 060-8628, Japan

Abstract

Two heterogeneous catalysts were synthesized from aromatic amino acids. Asymmetric Michael addition reaction and Mannich reaction were catalyzed, and the product shows a high ee value.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Natural Science Foundation of Shandong Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Polymers and Plastics,Biochemistry,Bioengineering

Link

http://pubs.rsc.org/en/content/articlepdf/2023/PY/D3PY00045A

Reference38 articles.

1. Atroposelective Synthesis of Axially Chiral 4-Aryl α-Carbolines via N-Heterocyclic Carbene Catalysis