Nickel-Catalyzed Radical Heck-Type C(sp<sup>3</sup>)–C(sp<sup>2</sup>) Coupling Cascades Enabled by Bromoalkane-Directed 1,4-Aryl Shift: Access to Olefinated Arylalanines-Reference-Cited by-同舟云学术

Nickel-Catalyzed Radical Heck-Type C(sp³)–C(sp²) Coupling Cascades Enabled by Bromoalkane-Directed 1,4-Aryl Shift: Access to Olefinated Arylalanines

Published:2022-11-01 Issue:44 Volume:24 Page:8192-8196
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Jian¹,Hong Yu¹,Liu Yin-Ling¹,Tan Jing-Ying¹,Liu Hao-Miao¹,Dai Gang-Liang¹,Chen Shi-Lu²^ORCID,Liu Ting¹,Li Jin-Heng³^ORCID,Tang Shi¹^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Jishou University, Jishou 416000, China

2. Key Laboratory of Cluster Science of Ministry of Education, Beijing Institute of Technology, Beijing 100081, China

3. State Key Laboratory Base of Eco-Chemical Engineering, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c03250

Reference51 articles.

1. Synthesis of Aromatic Boronic Acids. Aldehydo Boronic Acids and a Boronic Acid Analog of Tyrosine1

2. d-Amino Acids Boost the Selectivity and Confer Supramolecular Hydrogels of a Nonsteroidal Anti-Inflammatory Drug (NSAID)

3. Design, synthesis, and mechanism study of dimerized phenylalanine derivatives as novel HIV-1 capsid inhibitors

4. Preparation of enantiomerically pure protected 4-oxo .alpha.-amino acids and 3-aryl .alpha.-amino acids from serine

5. Expedient Synthesis of Chiral α-Amino Acids through Nickel-Catalyzed Reductive Cross-Coupling

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