An organic photoredox catalyst promoted <i>para</i>-selective C–H amination of aryl oximes-Reference-Cited by-同舟云学术

An organic photoredox catalyst promoted para-selective C–H amination of aryl oximes

Published:2023 Issue:2 Volume:10 Page:335-341
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Cheng¹,Zhang Xue-jun²,Zhao Yan-Wei¹,Liu Qianqian¹,Cheng Hongli¹,Huang Zhibin¹,Zhao Yingsheng¹³^ORCID

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215123, P.R. China

2. Department of Orthopedic Surgery, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, Jiangsu, China

3. School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang 453000, P.R.China

Abstract

Direct C–H amination methods are essential because of the importance of aryl amine derivatives.

Funder

Major Basic Research Project of the Natural Science Foundation of the Jiangsu Higher Education Institutions

Priority Academic Program Development of Jiangsu Higher Education Institutions

Henan Normal University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D2QO01650H

Reference53 articles.

1. Biogenetically-Inspired Total Synthesis of Epidithiodiketopiperazines and Related Alkaloids

2. Copper-mediated aromatic amination reaction and its application to the total synthesis of natural products

3. Catalytic Methods for Aromatic C–H Amination: An Ideal Strategy for Nitrogen-Based Functional Molecules

4. Palladium-Catalyzed Aromatic Aminations with in situ Generated Aminostannanes

5. Palladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amides

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