Jump to main content
Jump to site search

Issue 1, 2011
Previous Article Next Article

Nickel-catalysed cross-coupling reaction of aryl(trialkyl)silanes with aryl chlorides and tosylates

Author affiliations

Abstract

Using highly stable, readily accessible, and recyclable 2-(2-hydroxyprop-2-yl)cyclohexyl-substituted arylsilanes activated by a mild carbonate base, nickel-catalysed silicon-based arylaryl cross-coupling reaction proceeds for the first time with inexpensive aryl chlorides and tosylates in a highly chemoselective manner.

Graphical abstract: Nickel-catalysed cross-coupling reaction of aryl(trialkyl)silanes with aryl chlorides and tosylates

Back to tab navigation

Supplementary files

Publication details

The article was received on 29 Jun 2010, accepted on 26 Jul 2010 and first published on 23 Aug 2010


Article type: Communication
DOI: 10.1039/C0CC02173C
Chem. Commun., 2011,47, 307-309

  •   Request permissions

    Nickel-catalysed cross-coupling reaction of aryl(trialkyl)silanes with aryl chlorides and tosylates

    S. Tang, M. Takeda, Y. Nakao and T. Hiyama, Chem. Commun., 2011, 47, 307
    DOI: 10.1039/C0CC02173C

Search articles by author

Spotlight

Advertisements