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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 28, 1998 - Issue 17
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Original Articles

Regioselective Catalytic Halogenation of Aromatic Substrates

B. P. Bandgar Organic Chem. Research Lab., School of Chemical Sciences, Swami Ramanand Teerth Marathwada University, Dnyanteerth, Vishnupuri, Post Box No. 87, Nanded, 431 602, (Maharashtra), India Fax:
&
Miss Neeta J. Nigal Dept. of Chem., P.V.P. College, Pravaranagar, (Loni), 413 713, Dist. A'nagar
Pages 3225-3229 | Accepted 17 Feb 1998, Published online: 23 Aug 2006

Citations (15)

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K. Kulangiappar, M. Anbukulandainathan & T. Raju. (2014) Nuclear Versus Side-Chain Bromination of 4-Methoxy Toluene by an Electrochemical Method. Synthetic Communications 44:17, pages 2494-2502.
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N. Narender, P. Srinivasu, S. J. Kulkarni & K. V. Raghavan. (2002) HIGHLY EFFICIENT, PARA-SELECTIVE OXYCHLORINATION OF AROMATIC COMPOUNDS USING POTASSIUM CHLORIDE AND OXONE®*. Synthetic Communications 32:2, pages 279-286.
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Articles from other publishers (13)

Vijay Shekar Pulusu, Chinna Rajanna Kamatala, Anil Kumar Mardhanpally, Hemanth Sriram Yelike, Yaku Gugulothu, Satish Kumar Mukka, Umesh Kumar Utkoor & Yadagiri Pulusu. (2022) Silica Supported Acids (SiO2-HClO4, SiO2-KHSO4) as Eco-Friendly Reuasble Catalysts for Bromination of Aromatic and Heteroaromatic Compounds Using KBr under Solvothermal and Solvent-Free Conditions. Silicon 14:13, pages 7781-7791.
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Zhilong Chen. (2022) Recent development of biomimetic halogenation inspired by vanadium dependent haloperoxidase. Coordination Chemistry Reviews 457, pages 214404.
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VIJAY SHEKAR PULUSU, CHINNA RAJANNA KAMATALA, UMESH KUMAR UTKOOR, MAASI REDDY NAGANNAGARI, HEMANTH SRIRAM YELIKE, SAMBA SHIVA RAO ARISHA & YAKU GUGULOTHU. (2022) Silica Supported Acids (HClO4-SiO2, KHSO4-SiO2) as Eco-friendly Reusable Catalysts for Bromodecarboxylation of α,β-Unsaturated Carboxylic Acids using KBr under Solvothermal and Solvent-Free Conditions. Asian Journal of Chemistry 34:3, pages 535-542.
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Balu Misal, Amey Palav, Prerna Ganwir & Ganesh Chaturbhuj. (2021) Activator free, expeditious and eco-friendly chlorination of activated arenes by N-chloro-N-(phenylsulfonyl)benzene sulfonamide (NCBSI). Tetrahedron Letters 63, pages 152689.
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Richard C. LarockRichard C. Larock & Li Zhang. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 22 .
Chung‐Yu ChenGopal Chandru SenadiMei‐Chun LiuJeh‐Jeng Wang. (2016) Halogenation of Arenes via an In situ Generated Hypohalous Acid from m ‐CPBA and HX: Mechanistic Insights from Cyclic Voltammetry . ChemistrySelect 1:10, pages 2207-2211.
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Hadi Adibi, Abdol R. Hajipour & Majid Hashemi. (2007) A convenient and regioselective oxidative bromination of electron-rich aromatic rings using potassium bromide and benzyltriphenylphosphonium peroxymonosulfate under nearly neutral reaction conditions. Tetrahedron Letters 48:7, pages 1255-1259.
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Laijin Tian, Zhicai Shang, Xiaoliang Zheng, Yuxi Sun, You Yu, Bochu Qian & Xueli Liu. (2005) Synthesis, characterization and biological activity of diphenyltin(IV) complexes of N ‐(3,5‐dibromosalicylidene)‐α‐amino acid and their diphenyltin dichloride adducts . Applied Organometallic Chemistry 20:1, pages 74-80.
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Jallal M. Gnaim & Roger A. Sheldon. (2005) Regioselective bromination of aromatic compounds with Br2/SO2Cl2 over microporous catalysts. Tetrahedron Letters 46:26, pages 4465-4468.
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S.P. Stanforth. 2005. Comprehensive Organic Functional Group Transformations II. Comprehensive Organic Functional Group Transformations II 561 594 .
Min Young Park, Seung Gak Yang, Vidyadhar Jadhav & Yong Hae Kim. (2004) Practical and regioselective brominations of aromatic compounds using tetrabutylammonium peroxydisulfate. Tetrahedron Letters 45:25, pages 4887-4890.
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. (2002) Bromination of Activated Arenes by Oxone？ and Sodium Bromide. Bulletin of the Korean Chemical Society 23:5, pages 773-775.
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B. P. BANDGAR & N. J. NIGAL. (2010) ChemInform Abstract: Synthetic Methods. Part 9. Regioselective Catalytic Halogenation of Aromatic Substrates.. ChemInform 29:48.
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