NHC–palladium-catalyzed ionic liquid-accelerated regioselective oxyarylation of alkynes with diaryl ethers-Reference-Cited by-同舟云学术

NHC–palladium-catalyzed ionic liquid-accelerated regioselective oxyarylation of alkynes with diaryl ethers

Published:2022 Issue:5 Volume:24 Page:1983-1988
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Li Jianxiao¹²^ORCID,He Dan¹,Lin Zidong¹,Cen Liying¹,Wu Wanqing¹^ORCID,Jiang Huanfeng¹^ORCID

Affiliation:

1. Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou 510640, P. R. China

2. Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou 510640, China

Abstract

A palladium-catalyzed regioselective oxyarylation of oxime ether with diaryl ethers in a task-specific ionic liquid as an environmentally benign medium was accomplished.

Funder

Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology

Guangdong Science and Technology Department

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/GC/D1GC04556C

Reference50 articles.

1. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts