Pd(<scp>ii</scp>)-Catalyzed atroposelective C–H olefination: synthesis of enantioenriched <i>N</i>-aryl peptoid atropisomers-Reference-Cited by-同舟云学术

Pd(ii)-Catalyzed atroposelective C–H olefination: synthesis of enantioenriched N-aryl peptoid atropisomers

Published:2023 Issue:90 Volume:59 Page:13518-13521
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Jiang Tian-Yu¹,Ke Yi-Ting¹,Wu Yong-Jie¹,Yao Qi-Jun¹,Shi Bing-Feng¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry, Zhejiang University, Hangzhou, Zhejiang, 310027, China

2. School of Biotechnology and Health Sciences, Wuyi University, Jiangmen, Guangdong 529020, China

3. Green Catalysis Center, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China

4. College of Biological, Chemical Science and Engineering, Jiaxing University, Jiaxing 314001, China

Abstract

The synthesis of N-aryl peptoid atropisomers via Pd(ii)-catalyzed atroposelective C–H olefination using commercially available l-pGlu-OH as the chiral ligand was reported.

Funder

Natural Science Foundation of Zhejiang Province

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Science and Technology Department of Zhejiang Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC04425D

Reference46 articles.

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2. Peptoid architectures: elaboration, actuation, and application

3. Peptoid origins

4. Programming Amphiphilic Peptoid Oligomers for Hierarchical Assembly and Inorganic Crystallization

5. Folded biomimetic oligomers for enantioselective catalysis

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