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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 39, 2009 - Issue 4
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Original Articles

One-Pot Synthesis of Phenacyl Esters from Acetophenone, [Bmim]Br3, and Potassium Salts of Carboxylic Acids Under Solvent-Free Conditions

Zhang-Gao Le Department of Applied Chemistry, East China Institute of Technology, Fuzhou, ChinaCorrespondence[email protected]
,
Zong-Bo Xie Department of Applied Chemistry, East China Institute of Technology, Fuzhou, China
&
Jian-Ping Xu Department of Applied Chemistry, East China Institute of Technology, Fuzhou, China
Pages 743-747 | Received 03 May 2008, Published online: 27 Jan 2009

Citations (6)

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Javad Safaei-Ghomi & Mohammad Ali Ghasemzadeh. (2012) Preparation of 4,6-Diaryl-3,4-dihydropyrimidine-2(1H)-thiones in an Ionic Liquid. Organic Preparations and Procedures International 44:6, pages 527-531.
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Articles from other publishers (5)

Bapurao D. Rupanawar, Kishor D. Mane & Gurunath Suryavanshi. (2022) Hypervalent-iodine-mediated oxidation followed by the acetoxylation/tosylation of α-substituted benzylamines to obtain α-acyloxy/tosyloxy ketones. New Journal of Chemistry 46:35, pages 16832-16839.
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Richard C. LarockRichard C. Larock & Tuanli Yao. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 85 .
B.S. Sanatkumar, Jagannath Nayak & A. Nityananda Shetty. (2012) Influence of 2-(4-chlorophenyl)-2-oxoethyl benzoate on the hydrogen evolution and corrosion inhibition of 18 Ni 250 grade weld aged maraging steel in 1.0 M sulfuric acid medium. International Journal of Hydrogen Energy 37:11, pages 9431-9442.
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Hoong-Kun Fun, Tara Shahani, B. Garudachari, Arun M. Isloor & M. N. Satyganarayan. (2011) 2-(4-Chlorophenyl)-2-oxoethyl benzoate. Acta Crystallographica Section E Structure Reports Online 67:7, pages o1802-o1802.
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Zhang‐Gao Le, Zong‐Bo Xie & Jian‐Ping Xu. (2009) ChemInform Abstract: One‐Pot Synthesis of Phenacyl Esters from Acetophenone, [Bmim]Br 3 , and Potassium Salts of Carboxylic Acids under Solvent‐Free Conditions. . ChemInform 40:32.
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