A Mild Synthesis of 2-Substituted Benzothiazoles via Nickel-Catalyzed Intramolecular Oxidative C–H Functionalization-Reference-Cited by-同舟云学术

A Mild Synthesis of 2-Substituted Benzothiazoles via Nickel-Catalyzed Intramolecular Oxidative C–H Functionalization

Published:2019-12-17 Issue:2 Volume:85 Page:493-500
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gao Ming-Yuan¹,Li Jing-Hang¹,Zhang Shi-Bo¹,Chen Li-Jun¹,Li Yue-Sheng²,Dong Zhi-Bing²¹^ORCID

Affiliation:

1. School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, China

2. Hubei Key Laboratory of Radiation Chemistry and Functional Materials, School of Nuclear Technology and Chemistry & Biology, Hubei University of Science and Technology, Xianning 437100, China

Funder

Hubei Key Laboratory of Radiation Chemistry and Functional Materials, Hubei University of Science and Technology

MOE Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University

Hubei Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02543

Reference53 articles.

1. Oxidative Coupling between Two Hydrocarbons: An Update of Recent C–H Functionalizations

2. Intermolecular oxidative cross-coupling of arenes

3. Metal-free or transition-metal-catalyzed one-pot synthesis of 2-aminobenzothiazoles

4. Practical Synthesis of a Vanilloid Receptor-1 Antagonist

5. Organic phosphorus compounds. Part 3. Synthesis of 5-fluorosubstituted benzothiazolylbenzylphosphonates

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