Formate and CO<sub>2</sub> Enable Reductive Carboxylation of Imines: Synthesis of Unnatural α-Amino Acids-Reference-Cited by-同舟云学术

Formate and CO₂ Enable Reductive Carboxylation of Imines: Synthesis of Unnatural α-Amino Acids

Published:2024-06-28 Issue:14 Volume:89 Page:9750-9754
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Xu Pei¹,Liu Wen-Wen¹,Hao Tian-Zi¹,Liu Yi-Qin¹,Jiang Hui-Xian¹,Xu Jing¹,Li Jin-You¹,Yin Long¹,Zhu Song-Lei¹,Zhu Xu¹²^ORCID

Affiliation:

1. Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, School of Pharmacy, Xuzhou Medical University, Xuzhou 221004, China

2. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China

Funder

Natural Science Foundation of Jiangsu Province

Xuzhou Medical University

National Natural Science Foundation of China

Jiangsu Specially-Appointed Professor program

Natural Science Research Project of Jiangsu Universities

Jiangsu Province Shuangchuang Ph.D award

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c02887

Reference32 articles.

1. From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization Reactions

2. Enantiospecific Synthesis of Heterocycles from α-Amino Acids

3. Electrocarboxylation of N-Acylimines with Carbon Dioxide: Access to Substituted α-Amino Acids

4. Access to α-Arylglycines by Umpolung Carboxylation of Aromatic Imines with Carbon Dioxide

5. Catalytic Enantioselective Strecker Reactions and Analogous Syntheses

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1. α-Amino Acids by Reductive Carboxylation of Imines Using Formate and CO2;Synfacts;2024-09-13