Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 8, 2016
Previous Article Next Article

An efficient water-soluble surfactant-type palladium catalyst for Suzuki cross-coupling reactions in pure water at room temperature

Author affiliations

Abstract

A palladium catalyst based on a bidentate phosphine-type zwitterionic surfactant as a ligand exhibited an excellent catalytic activity in the Suzuki–Miyaura cross coupling reactions. This novel method allowed the reaction of aryl halides with arylboronic acids to occur in pure water at room temperature, forming a variety of biaryls in good to high yields. Heterobiaryls were also efficiently assembled even in the presence of water-insoluble heteroaryl halides as substrates. In addition, such a coupling protocol was successfully used in the iterative diarylation of 2,5-dibromopyridine in one-pot.

Graphical abstract: An efficient water-soluble surfactant-type palladium catalyst for Suzuki cross-coupling reactions in pure water at room temperature

Back to tab navigation

Supplementary files

Article information


Submitted
03 Feb 2016
Accepted
06 Jun 2016
First published
07 Jun 2016

New J. Chem., 2016,40, 6568-6572
Article type
Letter

An efficient water-soluble surfactant-type palladium catalyst for Suzuki cross-coupling reactions in pure water at room temperature

P. Qiu, J. Y. Zhao, X. Shi and X. H. Duan, New J. Chem., 2016, 40, 6568
DOI: 10.1039/C6NJ00377J

Social activity

Search articles by author

Spotlight

Advertisements