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Highly efficient α-arylation of aryl ketones with aryl chlorides by using bulky imidazolylidene-ligated oxazoline palladacycles.
Wei, Xian; Wang, Kun; Fang, Weiwei.
Afiliação
  • Wei X; 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. wwfang2020@njfu.edu.cn.
  • Wang K; 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. wwfang2020@njfu.edu.cn.
  • Fang W; 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. wwfang2020@njfu.edu.cn.
Org Biomol Chem ; 21(18): 3858-3862, 2023 May 10.
Article em En | MEDLINE | ID: mdl-37093227
ABSTRACT
α-Aryl derivatives of carbonyl compounds are important building blocks. Herein, we presented an efficient catalytic system for the α-arylation of aryl ketones with inactive aryl chlorides by firstly using N,N'-bis(2,6-diisopropylphenyl)-imidazol-2-ylidene (IPr)-ligated chiral oxazoline palladacycles, and tolerated a wide range of substrates at low catalyst loadings, leading to the desired products in good to excellent yields.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article