Oxidative Nickel-Catalyzed <i>ortho</i>-C–H Amination of (Iso)quinolines with Alicyclic Amines Directed by a Sacrificial <i>N</i>-Oxide Group-Reference-Cited by-同舟云学术

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Oxidative Nickel-Catalyzed ortho-C–H Amination of (Iso)quinolines with Alicyclic Amines Directed by a Sacrificial N-Oxide Group

Published:2024-01-25 Issue:4 Volume:26 Page:912-916
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zhu Weiqi¹,Wei Min¹,Wang Yanrui¹,Wang Guo¹,Wang Jianchun¹^ORCID,Rao Honghua¹²^ORCID

Affiliation:

1. Department of Chemistry, Capital Normal University, Beijing 100048, P. R. China

2. Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry, Tsinghua University, Beijing 100084, P. R. China

Funder

National Natural Science Foundation of China

Capital Normal University

MOE Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c04193

Reference47 articles.

1. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

2. Transition Metal-Catalyzed C–H Amination: Scope, Mechanism, and Applications

3. Mild metal-catalyzed C–H activation: examples and concepts

4. Heterocycle Formation via Palladium-Catalyzed C-H Functionalization

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