Skip to Content
MilliporeSigma
  • Copper-catalyzed ortho-acylation of phenols with aryl aldehydes and its application in one-step preparation of xanthones.

Copper-catalyzed ortho-acylation of phenols with aryl aldehydes and its application in one-step preparation of xanthones.

Chemical communications (Cambridge, England) (2012-10-17)
Jun Hu, Enoch A Adogla, Yong Ju, Daping Fan, Qian Wang
ABSTRACT

In the presence of triphenylphosphine, copper(II) chloride can catalyze an intermolecular ortho-acylation reaction of phenols with aryl aldehydes. The reaction proceeds smoothly with a wide range of starting materials, and furthermore, it can be used to synthesize xanthone derivatives in a single step in high yields.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Triphenylphosphine, ReagentPlus®, 99%
Sigma-Aldrich
Triphenylphosphine, ≥95.0% (GC)