Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 27th March 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 29, 2011
Previous Article Next Article

A versatile palladium catalyst system for Suzuki–Miyaura coupling of alkenyl tosylates and mesylates

Author affiliations

Abstract

A general and effective palladium system for Suzuki–Miyaura coupling of alkenyl electrophiles under mild reaction conditions is reported. With the Pd(OAc)2/CM-phos system, a variety of alkenyl tosylates are coupled well with ArB(OH)2. Moreover, the first successful examples of using alkenyl mesylates in alkenylation are also described.

Graphical abstract: A versatile palladium catalyst system for Suzuki–Miyaura coupling of alkenyl tosylates and mesylates

Back to tab navigation

Supplementary files

Publication details

The article was received on 18 Apr 2011, accepted on 25 May 2011 and first published on 17 Jun 2011


Article type: Communication
DOI: 10.1039/C1CC12240A
Citation: Chem. Commun., 2011,47, 8328-8330

  •   Request permissions

    A versatile palladium catalyst system for Suzuki–Miyaura coupling of alkenyl tosylates and mesylates

    P. Y. Wong, W. K. Chow, K. H. Chung, C. M. So, C. P. Lau and F. Y. Kwong, Chem. Commun., 2011, 47, 8328
    DOI: 10.1039/C1CC12240A

Search articles by author

Spotlight

Advertisements