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C. A. Marques, M. Selva and P. J. Tundo, “Facile Hydrodehalogenation with H2 and Pd/C Catalyst under Multiphase Conditions. 3. Selective Removal of Halogen from Functionalized Aryl Ketones. 4. Aryl Halide-Promoted Reduction of Benzyl Alcohols to Alkanes,” The Journal of Organic Chemistry, Vol. 60, 1995, pp. 2430-2435. doi:10.1021/jo00113a024

has been cited by the following article:

• TITLE: Efficient and Clean Catalytic Hydrogenolysis of Aromatic Ketones by Silica Supported Schiff Base Modify Chitosan-Palladium Catalyst

  AUTHORS: Tingting Gu, Lijun Liu, Changqiu Zhao

  KEYWORDS: CS-Schiff-Base; Pd Catalyst; Hydrogen; Aromatic Ketones

  JOURNAL NAME: Modern Research in Catalysis, Vol.2 No.1, January 28, 2013

  ABSTRACT: An silica supported chitosan-Schiff base Pd(II) catalyst was prepared in a simple way and characterized by XRD, FT-IR, SEM-EDS, XPS and TG, and the ability of this complex to catalyze hydrogenolysis of 1-tetralone into 1,2,3,4-tetrahydronaphthalene was also investigated in the presence of hydrogen. It has been revealed that the catalyst had high catalytic activity for hydrogenolysis of 1-tetralone at ambient temperature and normal pressure of hydrogen. Especially, the hydrogenolysis of 1-tetralone in ethanol solvent gave excellent results and the 100% conversion of 1-tetralone and the 100% selectivity for 1,2,3,4-tetrahydronaphthalene were obtained under optimized reaction conditions. The influences of reaction temperature, reaction time and solvent on the hydrogenolysis of 1-tetralone were also investigated. It has been also revealed that the catalyst was efficient and eco-friendly for the hydrogenolysis of carbonyl that connected with a benzene ring to give corresponding aromatic hydrocarbons.