From Anilines to Aryl Ethers: A Facile, Efficient, and Versatile Synthetic Method Employing Mild Conditions-Reference-Cited by-同舟云学术

From Anilines to Aryl Ethers: A Facile, Efficient, and Versatile Synthetic Method Employing Mild Conditions

Published:2018-03-06 Issue:14 Volume:57 Page:3641-3645
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Wang Dong-Yu¹²,Yang Ze-Kun³⁴,Wang Chao³⁴,Zhang Ao¹²⁵,Uchiyama Masanobu³⁴^ORCID

Affiliation:

1. CAS Key Laboratory of Receptor Research and the State Key Laboratory of Drug Research; Shanghai Institute of Materia Medica (SIMM); Chinese Academy of Sciences; Shanghai 201203 China

2. University of Chinese Academy of Sciences; Beijing 100049 China

3. Graduate School of Pharmaceutical Sciences; University of Tokyo; 7-3-1 Hongo Bunkyo-ku Tokyo 113-0033 Japan

4. Elements Chemistry Laboratory; RIKEN; 2-1 Hirosawa Wako-shi Saitama 351-0198 Japan

5. School of Life Science and Technology, ShanghaiTech University; Shanghai 201210 China

Funder

Chinese NSF

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference56 articles.

1. Transition-Metal-Catalyzed Cleavage of C–N Single Bonds

2. Cleavage of C−N Bonds in Aniline Derivatives on a Ruthenium Center and Its Relevance to Catalytic C−C Bond Formation

3. Nickel-Catalyzed Reductive and Borylative Cleavage of Aromatic Carbon–Nitrogen Bonds in N-Aryl Amides and Carbamates

4. C−N Bond Activation and Ring Opening of a Saturated N-Heterocyclic Carbene by Lateral Alkali-Metal-Mediated Metalation

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