Issue 36, 2014
From the journal:

Organic & Biomolecular Chemistry

MIDA as a simple and highly efficient ligand for palladium-catalyzed Hiyama cross-coupling of aryl halides†

Mengping Guo,*ab   Liang Qi,ab   Qiaochu Zhang,ab   Zhiyong Zhu,a   Wei Lia  and  Xiaogang Liab  

* Corresponding authors

a Institute of Coordination Catalysis, College of Chemistry and Bio-engineering, Yichun University, Yichun 336000, PR China
E-mail: guomengping65@163.com

b Engineering Center of Jiangxi University for Lithium Energy, Yichun University, Yichun 336000, PR China

Abstract

N-Methyliminodiacetic acid (MIDA) as a simple, air stable and water-soluble ligand has been used in the palladium-catalyzed Hiyama cross-coupling reaction of trimethoxyphenylsilane with aryl halides. The yield of the corresponding Hiyama coupling products is high up to around 90% in water and isopropanol under an ambient atmosphere in the presence of KOH and NaF.

Graphical abstract: MIDA as a simple and highly efficient ligand for palladium-catalyzed Hiyama cross-coupling of aryl halides

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C4OB01056F
Article type
Paper
Submitted
22 May 2014
Accepted
24 Jul 2014
First published
11 Aug 2014

Org. Biomol. Chem., 2014,12, 7136-7139

Permissions

Request permissions

MIDA as a simple and highly efficient ligand for palladium-catalyzed Hiyama cross-coupling of aryl halides

M. Guo, L. Qi, Q. Zhang, Z. Zhu, W. Li and X. Li, Org. Biomol. Chem., 2014, 12, 7136 DOI: 10.1039/C4OB01056F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements