Jump to main content
Jump to site search

Issue 17, 2015
Previous Article Next Article

Nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes

Author affiliations

Abstract

A nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes using removable 2-(pyridine-2-yl)-isopropylamine as a directing group is described. This strategy provides an efficient access to valuable aryl sulfides with ample substrate scope and a high degree of functional group tolerance.

Graphical abstract: Nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes

Back to tab navigation

Supplementary files

Publication details

The article was received on 31 Dec 2014, accepted on 22 Jan 2015 and first published on 23 Jan 2015


Article type: Communication
DOI: 10.1039/C4CC10431E
Author version
available:
Download author version (PDF)
Chem. Commun., 2015,51, 3582-3585

  •   Request permissions

    Nickel-catalyzed and benzoic acid-promoted direct sulfenylation of unactivated arenes

    K. Yang, Y. Wang, X. Chen, A. A. Kadi, H. Fun, H. Sun, Y. Zhang and H. Lu, Chem. Commun., 2015, 51, 3582
    DOI: 10.1039/C4CC10431E

Search articles by author

Spotlight

Advertisements