Jump to main content
Jump to site search

Issue 8, 2018
Previous Article Next Article

Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki–Miyaura coupling reactions

Author affiliations

Abstract

A series of new monophosphine ligands containing a naphthofuran skeleton have been prepared, characterized and evaluated in palladium-catalyzed Suzuki–Miyaura coupling reactions. Using Pd2(dba)3L6 as the catalyst the reactions were performed with high catalytic activity under mild reaction conditions and the desired coupling products were obtained in good to excellent yields. The new catalyst system also showed broad substrate adaptability and practicality for gram-scale production.

Graphical abstract: Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki–Miyaura coupling reactions

Back to tab navigation

Supplementary files

Publication details

The article was received on 23 Jan 2018, accepted on 09 Mar 2018 and first published on 13 Mar 2018


Article type: Paper
DOI: 10.1039/C8NJ00412A
Citation: New J. Chem., 2018,42, 5967-5971
  •   Request permissions

    Synthesis of a class of binaphthyl monophosphine ligands with a naphthofuran skeleton and their applications in Suzuki–Miyaura coupling reactions

    Z. Zhou, H. Liang, W. Xia, H. Chen, Y. Zhang, X. He, S. Yu, R. Cao and L. Qiu, New J. Chem., 2018, 42, 5967
    DOI: 10.1039/C8NJ00412A

Search articles by author

Spotlight

Advertisements