Direct Asymmetric α-Alkylation of NH<sub>2</sub>-Unprotected Amino Acid Esters Enabled by Biomimetic Chiral Pyridoxals-Reference-Cited by-同舟云学术

Direct Asymmetric α-Alkylation of NH₂-Unprotected Amino Acid Esters Enabled by Biomimetic Chiral Pyridoxals

Published:2023-06-26 Issue:13 Volume:13 Page:9150-9157
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Ji Pengwei¹,Li Jianyu¹^ORCID,Tao Yuhang¹,Li Mingzhe¹,Ling Weibo¹,Chen Jianfeng¹,Zhao Baoguo¹^ORCID

Affiliation:

1. The Education Ministry Key Lab of Resource Chemistry, Shanghai Key Laboratory of Rare Earth Functional Materials, and Shanghai Frontiers Science Center of Biomimetic Catalysis, Shanghai Normal University, Shanghai 200234, China

Funder

Shanghai Municipal Education Commission

Science and Technology Commission of Shanghai Municipality

National Natural Science Foundation of China

Shanghai Engineering Research Center of Green Energy Chemical Engineering, Shanghai Normal University

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.3c01770

Reference69 articles.

1. Protecting Group Strategies in Organic Synthesis

2. Protecting-group-free synthesis as an opportunity for invention

3. LiOH-mediated N -monoalkylation of α-amino acid esters and a dipeptide ester using activated alkyl bromides

4. The Enantioselective Synthesis of α-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters

5. Recent progress on the stereoselective synthesis of acyclic quaternary α-amino acids

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