Issue 48, 2016

Nickel-catalyzed α-benzylation of sulfones with esters via C–O activation

Abstract

The nickel-catalyzed α-benzylation of sulfones with readily available benzylic alcohol derivatives was achieved via C–O activation. The transformation was complete in 30 minutes using a simple Ni(COD)2 as a catalyst without any additional ligands. A variety of substituted sulfones including the building block for bioactive compound eletriptan were synthesized by using the strategy.

Graphical abstract: Nickel-catalyzed α-benzylation of sulfones with esters via C–O activation

Supplementary files

Article information

Article type
Communication
Submitted
18 Mar 2016
Accepted
18 Apr 2016
First published
20 Apr 2016

RSC Adv., 2016,6, 42656-42659

Nickel-catalyzed α-benzylation of sulfones with esters via C–O activation

J. Xiao, J. Yang, T. Chen and L. Han, RSC Adv., 2016, 6, 42656 DOI: 10.1039/C6RA07130A

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