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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 34, 2004 - Issue 4
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Original Articles

Pd/C‐Catalyzed Transfer‐Hydrogenation of Benzaldehydes to Benzyl Alcohols Using Potassium Formate as the Selective Hydrogen Donor

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Pages 643-650 | Received 14 Aug 2003, Published online: 16 Aug 2006

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Anwei Wang, Zhiyong Yang, Jidan Liu, Qingwen Gui, Xiang Chen, Ze Tan & Ji-Cheng Shi. (2014) Pd-Catalyzed Reduction of Aldehydes to Alcohols Using Formic Acid as the Hydrogen Donor. Synthetic Communications 44:2, pages 280-288.
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Articles from other publishers (22)

Zi-Jie Gong, Yemineni S.L.V. Narayana, Yen-Chun Lin, Wei-Hsiang Huang, Wei-Nien Su, Yi-Pei Li, Masayoshi Higuchi & Wen-Yueh Yu. (2022) Rational synthesis of ruthenium-based metallo-supramolecular polymers as heterogeneous catalysts for catalytic transfer hydrogenation of carbonyl compounds. Applied Catalysis B: Environmental 312, pages 121383.
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Ashish Bahuguna, Sourav Chakraborty & Yoel Sasson. (2021) NiO–Ni/graphitic carbon nitride as a selective catalyst for transfer hydrogenation of carbonyl compounds using NaH2PO2 as a hydrogen source. International Journal of Hydrogen Energy 46:56, pages 28554-28564.
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Kirill A. Korvinson, Hari K. Akula, Casina T. Malinchak, Dellamol Sebastian, Wei Wei, Tashrique A. Khandaker, Magdalena R. Andrzejewska, Barbara Zajc & Mahesh K. Lakshman. (2019) Catalytic Reductions Without External Hydrogen Gas: Broad Scope Hydrogenations with Tetrahydroxydiboron and a Tertiary Amine. Advanced Synthesis & Catalysis 362:1, pages 166-176.
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Wanwitoo Wanmolee, Jorge N. Beltramini, Luqman Atanda, John P. Bartley, Navadol Laosiripojana & William O. S. Doherty. (2019) Effect of HCOOK/Ethanol on Fe/HUSY, Ni/HUSY, and Ni–Fe/HUSY Catalysts on Lignin Depolymerization to Benzyl Alcohols and Bioaromatics. ACS Omega 4:16, pages 16980-16993.
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Priti Sharma & Yoel Sasson. (2019) Sustainable visible light assisted in situ hydrogenation via a magnesium–water system catalyzed by a Pd-g-C 3 N 4 photocatalyst . Green Chemistry 21:2, pages 261-268.
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Richard C. LarockRichard C. Larock & Cristiano Raminelli. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 69 .
Swechchha Pandey, Dinesh R. Shinde & Samir H. Chikkali. (2017) Isomerizing Hydroformylation of Cashew Nut Shell Liquid. ChemCatChem 9:20, pages 3997-4004.
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Roman M. Mironenko, Olga B. Belskaya, Tatyana I. Gulyaeva, Mikhail V. Trenikhin, Alexander I. Nizovskii, Alexander V. Kalinkin, Valerii I. Bukhtiyarov, Alexander V. Lavrenov & Vladimir A. Likholobov. (2017) Liquid-phase hydrogenation of benzaldehyde over Pd-Ru/C catalysts: Synergistic effect between supported metals. Catalysis Today 279, pages 2-9.
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Jayesh T. Bhanushali, Itika Kainthla, Rangappa S. Keri & Bhari Mallanna Nagaraja. (2016) Catalytic Hydrogenation of Benzaldehyde for Selective Synthesis of Benzyl Alcohol: A Review. ChemistrySelect 1:13, pages 3839-3853.
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Feng Jiang, Jian Cai, Bing Liu, Yuebing Xu & Xiaohao Liu. (2016) Particle size effects in the selective hydrogenation of cinnamaldehyde over supported palladium catalysts. RSC Advances 6:79, pages 75541-75551.
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Roman M. Mironenko, Olga B. Belskaya, Vladimir I. Zaikovskii & Vladimir A. Likholobov. (2015) Effects of the carbon support nature and ruthenium content on the performances of Ru/C catalysts in the liquid-phase hydrogenation of benzaldehyde to benzyl alcohol. Monatshefte für Chemie - Chemical Monthly 146:6, pages 923-930.
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Yanxiu Gao, Stephan Jaenicke & Gaik-Khuan Chuah. (2014) Highly efficient transfer hydrogenation of aldehydes and ketones using potassium formate over AlO(OH)-entrapped ruthenium catalysts. Applied Catalysis A: General 484, pages 51-58.
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Maoshuai Li, Xiaodong Wang, Noémie Perret & Mark A. Keane. (2014) Enhanced production of benzyl alcohol in the gas phase continuous hydrogenation of benzaldehyde over Au/Al2O3. Catalysis Communications 46, pages 187-191.
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O. B. Belskaya, R. M. Mironenko & V. A. Likholobov. (2013) Effect of carbon support nature and palladium content on the properties of Pd/C catalysts in hydrogenation of benzaldehyde. Theoretical and Experimental Chemistry 48:6, pages 381-385.
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Shinya Yoshida, Makoto Kasai, Takenori Kimura, Takahiro Akiba, Takumi Takahashi & Shuichi Sakamoto. (2012) Development of a Practical and Scalable Synthesis of a Potent Selective Dual Antagonist for 5-HT2B and 5-HT7 Receptors. Organic Process Research & Development 16:4, pages 654-663.
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Leyla Pehlivan, Estelle Métay, Olivier Boyron, Patrice Demonchaux, Gérard Mignani & Marc Lemaire. (2011) A New Solvent‐Free Reaction for the Preparation of Alkoxysilane from Cyclic Ethers, Alcohols, or Carbonyl Compounds. European Journal of Organic Chemistry 2011:24, pages 4687-4692.
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Z. S. Liu & G. L. Rempel. (2010) Kinetic study of hydrogen transfer from benzyl alcohol to aliphatic aldehydes catalysed by heterogenised ruthenium(II) catalysts. The Canadian Journal of Chemical Engineering, pages n/a-n/a.
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Lin He, Ji Ni, Lu‐Cun Wang, Feng‐Jiao Yu, Yong Cao, He‐Yong He & Kang‐Nian Fan. (2009) Aqueous Room‐Temperature Gold‐Catalyzed Chemoselective Transfer Hydrogenation of Aldehydes. Chemistry – A European Journal 15:44, pages 11833-11836.
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Z.S. Liu & G.L. Rempel. (2007) The triphasic transfer hydrogenation of aromatic aldehydes by aqueous sodium formate in the presence of heterogenized ruthenium(II) complexes bound to swellable polymer matrices. Journal of Molecular Catalysis A: Chemical 278:1-2, pages 228-236.
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Malhari D. Bhor, Mayur J. Bhanushali, Nitin S. Nandurkar & Bhalchandra M. Bhanage. (2007) Highly efficient chemoselective catalytic hydrogenation of diaryl substituted α,β-unsaturated nitriles/carbonyls using homogeneous Pd(OAc)2/PPh3 catalyst. Catalysis Communications 8:12, pages 2064-2068.
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Michael P. WilsonNathaniel W. AlcockP. Mark Rodger. (2006) Structure of Anhydrous Alkali-Metal Formates. Inorganic Chemistry 45:11, pages 4359-4363.
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Mubeen Baidossi, Ashutosh V. Joshi, Sudip Mukhopadhyay & Yoel Sasson. (2004) Pd/C‐Catalyzed Transfer‐Hydrogenation of Benzaldehydes to Benzyl Alcohols Using Potassium Formate as the Selective Hydrogen Donor.. ChemInform 35:31.
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