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Wagh, Y.S., Sawant, D.N., Tambada, P.J., Dhake, K.P. and Bhanage, B.M. (2011) Pd(OAc)2/Dppf as an Efficient and Highly Active Catalyst for the Allylation of Amines, Alcohols and Carboxylic Acids with 1-Phenyl-1-Propyne. Tetrahedron, 67, 2414-2421.
https://doi.org/10.1016/j.tet.2011.02.008

has been cited by the following article:

• TITLE: Liquid Etherification of Alkoxybenzyl Alcohols, Cinnamyl Alcohols and Fluorinated Phenylalkenols with Platinum on Carbon (Pt/C) and Palladium on Carbon (Pd/C)

  AUTHORS: Thies Thiemann

  KEYWORDS: Benzyl Alcohols, Etherification, Platinum on Carbon, Palladium on Carbon, Activated Carbon, Solvent Free Reaction

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.8 No.1, March 6, 2018

  ABSTRACT: In the presence of either Pd/C or Pt/C, 4-alkoxybenzyl alcohols, 4-alkoxy-phenylalkyl alcohols and cinnamyl alcohols undergo liquid etherification to bis(4-alkoxybenzyl) ethers, bis[(4-alkoxybenzyl)alkyl] ethers and bis(cin-namyl) ethers at temperatures of 100°C - 135°C. In a number of cases, Pt/C and Pd/C as catalysts, also when they are doped with Ru, show distinct differences when the reactions run in air, with an oxidative dehydrogenation of the alcohols as side-reaction, yielding the corresponding ketones and aldehydes as by-products. Also, the reactivity of fluorinated phenylalkenols under these conditions has been investigated. Furthermore, the immobilization of alkyl aryl ethers on silica within a column with passage of hexane as solvent was found to lead to the formation and elution of styrenes from the column in fair yield.