Highly efficient α-arylation of aryl ketones with aryl chlorides by using bulky imidazolylidene-ligated oxazoline palladacycles-Reference-Cited by-同舟云学术

Highly efficient α-arylation of aryl ketones with aryl chlorides by using bulky imidazolylidene-ligated oxazoline palladacycles

Published:2023 Issue:18 Volume:21 Page:3858-3862
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wei Xian¹,Wang Kun¹,Fang Weiwei¹^ORCID

Affiliation:

1. Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, International Innovation Center for Forest Chemicals and Materials, College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, China

Abstract

An efficient catalytic system for the α-arylation of aryl ketones with aryl chlorides by firstly using IPr-ligated oxazoline palladacycles was developed, which tolerated various substrates at low catalyst loadings and gave products in good yields.

Funder

Nanjing Forestry University

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00354J

Reference72 articles.

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