Issue 20, 2016

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

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

Supplementary files

Article information

Article type
Paper
Submitted
14 Jan 2016
Accepted
15 Apr 2016
First published
19 Apr 2016

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

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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