Preparation of Axially Chiral 2,2′-Biimidazole Ligands through Remote Chirality Delivery and Their Application in Asymmetric Carbene Insertion into N

Preparation of Axially Chiral 2,2′-Biimidazole Ligands through Remote Chirality Delivery and Their Application in Asymmetric Carbene Insertion into N–H of Carbazoles

Published:2019-03-28 Issue:8 Volume:21 Page:2712-2717
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Shen Hong-Qiang¹²,Wu Bo¹,Xie Huan-Ping¹,Zhou Yong-Gui¹³^ORCID

Affiliation:

1. State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, People’s Republic of China

2. University of Chinese Academy of Sciences, Beijing 100049, People’s Republic of China

3. Collaborative Innovation Centre of Chemical Science and Engineering, Tianjin 300071, People’s Republic of China

Funder

National Natural Science Foundation of China

Chinese Academy of Sciences

Dalian Institute of Chemical Physics

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00687

Reference64 articles.

1. Heterocycles in Life and Society

2. Chemistry of the Biologically Important Imidazoles.

3. Interactions of histidine and other imidazole derivatives with transition metal ions in chemical and biological systems

4. Biological Significance and Applications of Heme c Proteins and Peptides

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