Issue 20, 2016
From the journal:

Organic & Biomolecular Chemistry

An efficient indenyl-derived phosphine ligand for the Suzuki–Miyaura coupling of sterically hindered aryl halides†

Yan Liu,a   Hui Peng,a   Jia Yuan,a   Meng-Qi Yan,a   Xue Luo,a   Qing-Guo Wu,a   Sheng-Hua Liu,a   Jian Chen*a  and  Guang-Ao Yu*a  

* Corresponding authors

a Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, People's Republic of China
E-mail: jianc@mail.ccnu.edu.cn, yuguang@mail.ccnu.edu.cn

Abstract

An air-stable aryl substituted indenyl phosphine used in combination with Pd(OAc)2 provides a highly efficient catalyst for the Suzuki–Miyaura cross-coupling reaction of sterically hindered aryl halides with aryl boronic acids.

Graphical abstract: An efficient indenyl-derived phosphine ligand for the Suzuki–Miyaura coupling of sterically hindered aryl halides

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Article information

DOI
https://doi.org/10.1039/C6OB00096G
Article type
Paper
Submitted
14 Jan 2016
Accepted
15 Apr 2016
First published
19 Apr 2016

Org. Biomol. Chem., 2016,14, 4664-4668

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An efficient indenyl-derived phosphine ligand for the Suzuki–Miyaura coupling of sterically hindered aryl halides

Y. Liu, H. Peng, J. Yuan, M. Yan, X. Luo, Q. Wu, S. Liu, J. Chen and G. Yu, Org. Biomol. Chem., 2016, 14, 4664 DOI: 10.1039/C6OB00096G

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