Issue 20, 2015

Ni(ii) source as a pre-catalyst for the cross-coupling of benzylic pivalates with arylboronic acids: facile access to tri- and diarylmethanes

Abstract

A simple and easily-used NiII complex, Ni(PPh3)2(1-naphthyl)Cl, was employed as a pre-catalyst in the Suzuki–Miyaura cross-coupling of benzylic pivalates with arylboronic acids, affording various tri- or diarylmethanes in good yields under mild conditions. This new protocol provides a cheap, convenient and practical alternative to synthesizing multiaryl methanes.

Graphical abstract: Ni(ii) source as a pre-catalyst for the cross-coupling of benzylic pivalates with arylboronic acids: facile access to tri- and diarylmethanes

Supplementary files

Article information

Article type
Communication
Submitted
16 Dec 2014
Accepted
23 Jan 2015
First published
23 Jan 2015

RSC Adv., 2015,5, 15338-15340

Ni(II) source as a pre-catalyst for the cross-coupling of benzylic pivalates with arylboronic acids: facile access to tri- and diarylmethanes

Q. Chen, X. Fan, L. Zhang and L. Yang, RSC Adv., 2015, 5, 15338 DOI: 10.1039/C4RA16452K

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