Cyanide Ion-Promoted Nucleophilic Displacement of Aromatic Nitro Groups: A Mild, One-Pot, Transition Metal-Free Synthesis of Nitrile-Containing Naphthalimide Aryl Ether Derivatives-Reference-Cited by-同舟云学术

Cyanide Ion-Promoted Nucleophilic Displacement of Aromatic Nitro Groups: A Mild, One-Pot, Transition Metal-Free Synthesis of Nitrile-Containing Naphthalimide Aryl Ether Derivatives

Published:2021-01-12 Issue:3 Volume:86 Page:3059-3064
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chen Lu¹,Chen Xi¹,Zhu Tingting¹,Shao Haibing¹,Chen Zhihua¹,Hu Yan¹,Liu Zhenjiang¹^ORCID,Liu Chuanxiang¹^ORCID

Affiliation:

1. School of Chemical and Environmental Engineering, Shanghai Institute of Technology, Shanghai 201418, P. R. China

Funder

Natural Science Foundation of Shanghai

Shanghai Institute of Technology

Shanghai Key Laboratory of Chemical Biology

Chemical Engineering and Technology (Perfume and Aroma Technology) of Shanghai Plateau Discipline

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c02598

Reference31 articles.

1. Total Synthesis of Hirsutellone B

2. Cu-Catalyzed Arylation of Phenols: Synthesis of Sterically Hindered and Heteroaryl Diaryl Ethers

3. Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis

4. Modern Synthetic Methods for Copper-Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation

5. Catalytic CC, CN, and CO Ullmann-Type Coupling Reactions: Copper Makes a Difference

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