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  • 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
ZUSAMMENFASSUNG

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.

MATERIALIEN
Produktnummer
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Produktbeschreibung

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