Ni-catalyzed enantioselective three-component reductive alkylacylation of alkenes: modular access to structurally complex α-amino ketones-Reference-Cited by-同舟云学术

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Ni-catalyzed enantioselective three-component reductive alkylacylation of alkenes: modular access to structurally complex α-amino ketones

Published:2024 Issue: Volume: Page:
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Xiao Jichao¹^ORCID,Jia Tingting¹,Chen Shuang¹,Pan Mengxiao¹,Li Xingwei¹²^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, Shanxi 710062, China

2. Institute of Molecular Science and Engineering, Institute of Frontier and Interdisciplinary Sciences, Shandong University, Qingdao, Shandong 266237, China

Abstract

Nickel-catalyzed three-component reductive dicarbofunctionalization of activated olefins (enamides) is presented.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC04561K

Reference85 articles.

1. Synthesis and biological activity of a ketomethylene analog of a tripeptide inhibitor of angiotensin converting enzyme

2. A Short, One-Pot Synthesis of Bupropion (Zyban, Wellbutrin)

3. Synthesis of novel keto-ACE analogues as domain-selective angiotensin I-converting enzyme inhibitors

4. Synthesis and Biological Evaluation of Bupropion Analogues as Potential Pharmacotherapies for Cocaine Addiction

5. Transition Metal Catalyzed Enantioselective α-Heterofunctionalization of Carbonyl Compounds

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