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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 33, 2003 - Issue 14
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Original Articles

An Alternative Method for the Highly Selective Iodination of Alcohols Using a CsI/BF3·Et2O System

Safdar Hayat International Center for Chemical Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan
,
Atta-ur-Rahman International Center for Chemical Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan
,
Khalid Mohammed Khan International Center for Chemical Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, PakistanCorrespondence[email protected]
,
M. Iqbal Choudhary International Center for Chemical Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan
,
Ghulam Murtaza Maharvi International Center for Chemical Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan
,
Zia-Ullah International Center for Chemical Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan
&
Ernst Bayer International Center for Chemical Sciences, H. E. J. Research Institute of Chemistry, University of Karachi, Karachi, Pakistan
 show all
Pages 2531-2540 | Received 20 Sep 2002, Published online: 20 Aug 2006

Citations (12)

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Abdol Reza Hajipour, Majid Mostafavi & ArnoldE. Ruoho. (2009) Iodination of Alcohols using Triphenylphosphine/Iodine in Ionic Liquid under Solvent-Free Conditions. Organic Preparations and Procedures International 41:1, pages 87-91.
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Articles from other publishers (11)

Richard C. LarockRichard C. Larock & Li Zhang. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 24 .
Richard C. LarockRichard C. Larock & Li Zhang. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 19 .
Serena Traboni, Emiliano Bedini & Alfonso Iadonisi. (2018) Solvent-Free Conversion of Alcohols to Alkyl Iodides and One-Pot Elaborations Thereof. ChemistrySelect 3:6, pages 1616-1622.
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Burak Yıldız, Yasemin Baygu, İzzet Kara, Hakan Dal & Yaşar Gök. (2016) The synthesis, characterization and computional investigation of new metalloporphyrazine containing 15-membered S4 donor macrocyclic moieties. Tetrahedron 72:44, pages 6972-6981.
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DIPARJUN DAS, JASHA MOMO H ANAL & LALTHAZUALA ROKHUM. (2016) A mild and highly chemoselective iodination of alcohol using polymer supported DMAP. Journal of Chemical Sciences 128:11, pages 1695-1701.
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Leila Khazdooz, Amin Zarei, Hamidreza Aghaei, Ghobad Azizi & Mohammad Mehdi Gheisari. (2016) An efficient and selective method for the iodination and bromination of alcohols under mild conditions. Tetrahedron Letters 57:2, pages 168-171.
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Qing-Hai Deng, Hubert Wadepohl & Lutz H. Gade. (2012) Highly Enantioselective Copper-Catalyzed Alkylation of β-Ketoesters and Subsequent Cyclization to Spirolactones/Bi-spirolactones. Journal of the American Chemical Society 134:6, pages 2946-2949.
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Malhari D. Bhor, Anil G. Panda, Nitin S. Nandurkar & Bhalchandra M. Bhanage. (2008) Synthesis of alkyl iodides/nitriles from carbonyl compounds using novel ruthenium tris(2,2,6,6-tetramethyl-3,5-heptanedionate) as catalyst. Tetrahedron Letters 49:45, pages 6475-6479.
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Seetharamaiyer Padmanabhan, John E. Coughlin, Guangrong Zhang, Cassandra J. Kirk & Radhakrishnan P. Iyer. (2006) Anti-HBV nucleotide prodrug analogs: Synthesis, bioreversibility, and cytotoxicity studies. Bioorganic & Medicinal Chemistry Letters 16:6, pages 1491-1494.
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Brindaban C. Ranu & Ranjan Jana. (2005) Direct Halogenation of Alcohols and Their Derivatives with tert‐ Butyl Halides in the Ionic Liquid [pmIm]Br under Sonication Conditions – A Novel, Efficient and Green Methodology . European Journal of Organic Chemistry 2005:4, pages 755-758.
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Safdar Hayat, Atta‐ur‐Rahman Atta‐ur‐Rahman, Khalid Mohammed Khan, M. Iqbal Choudhary, Ghulam Murtaza Maharvi, Zia‐Ullah Zia‐Ullah & Ernst Bayer. (2003) An Alternative Method for the Highly Selective Iodination of Alcohols Using a CsI/BF 3 ×Et 2 O System. . ChemInform 34:46.
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