Nickel-catalysed C–N cross-coupling of organoboronic acids and isoxazoles-Reference-Cited by-同舟云学术

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Nickel-catalysed C–N cross-coupling of organoboronic acids and isoxazoles

Published:2024 Issue:18 Volume:11 Page:5138-5143
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhao Yupeng¹,Wu Changshu¹^ORCID,Zhang Jiaming¹,Gao Yang¹²^ORCID,Yuan Zhuoxuan¹,Li Xianwei¹^ORCID,Chen Qian¹^ORCID,Huo Yanping¹²^ORCID

Affiliation:

1. School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China

2. Jieyang Branch of Chemistry and Chemical Engineering Guangdong Laboratory, Jieyang 515200, China

Abstract

A nickel-catalyzed C–N cross-coupling of organoboronic acids and isoxazoles has been established for the efficient synthesis of (Z) N-aryl β-enamino esters.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO01050G

Reference53 articles.

1. Total synthesis of kottamide E

2. Total Synthesis of the Salicylate Enamide Macrolide Oximidine II

3. Marine natural products

4. Lewis Acid-Relayed Singlet Oxygen Reaction with Enamines: Selective Dimerization of Enamines to Pyrrolin-4-ones

5. Cu(TFA)2-Catalyzed Oxidative Tandem Cyclization/1,2-Alkyl Migration of Enamino Amides for Synthesis of Pyrrolin-4-ones

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