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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 12, 1982 - Issue 14
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Original Articles

Studies on Reactivity of Pyridinium Chlorochromate — Iodine System: An Efficient Method for Converting Enol Silyl Ethers into α-Iodo Ketones

Maurizio D'auria Centro CNR per lo Studio della Chimica delle Sostanze Organiche Naturali c/o Istituto di Chimica Organica, Università di Roma, P. le A. Moro. 2, 00185, Roma, Italy
,
Franco D'onofrio Centro CNR per lo Studio della Chimica delle Sostanze Organiche Naturali c/o Istituto di Chimica Organica, Università di Roma, P. le A. Moro. 2, 00185, Roma, Italy
,
Giovanni Piancatelli Centro CNR per lo Studio della Chimica delle Sostanze Organiche Naturali c/o Istituto di Chimica Organica, Università di Roma, P. le A. Moro. 2, 00185, Roma, Italy
&
Arrigo Scettri Centro CNR per lo Studio della Chimica delle Sostanze Organiche Naturali c/o Istituto di Chimica Organica, Università di Roma, P. le A. Moro. 2, 00185, Roma, Italy
Pages 1127-1138 | Published online: 05 Dec 2006

Citations (17)

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Darko Dolenc. (2003) Iodination of Enol Acetates and 1,3-Diones Using N-Iodosaccharin. Synthetic Communications 33:16, pages 2917-2924.
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FrederickA. Luzzio & FrankS. Guziec$suffix/text()$suffix/text(). (1988) RECENT APPLICATIONS OF OXOCHROMIUMAMINE COMPLEXES AS OXIDANTS IN ORGANIC SYNTHESIS. A REVIEW. Organic Preparations and Procedures International 20:6, pages 533-584.
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Articles from other publishers (15)

Richard C. LarockRichard C. Larock & Li Zhang. 2018. Comprehensive Organic Transformations. Comprehensive Organic Transformations 1 62 .
Melchior Menzel & Thomas Ziegler. (2014) Synthesis of Vicinal Diketoses by Using a Metathesis–Hydroxylation–Oxidation Sequence. European Journal of Organic Chemistry 2014:34, pages 7658-7663.
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Y. Obora & Y. Ishii. 2014. Comprehensive Organic Synthesis II. Comprehensive Organic Synthesis II 262 276 .
Rodrigo da S. Ribeiro, Pierre M. Esteves & Marcio C.S. de Mattos. (2007) Triiodoisocyanuric acid: a new and convenient reagent for regioselective coiodination of alkenes and enolethers with oxygenated nucleophiles. Tetrahedron Letters 48:49, pages 8747-8751.
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Giovanni Piancatelli & Frederick A. Luzzio. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Louis F. Fieser, Mary Fieser & Tse‐Lok HoTse‐Lok Ho, Mary Fieser & Louis Fieser. 2006. Fieser and Fieser's Reagents for Organic Synthesis. Fieser and Fieser's Reagents for Organic Synthesis.
Susan B. Billings & K. A. Woerpel. (2006) Nucleophilic Substitution Reactions of Sulfur-Substituted Cyclohexanone Acetals:  An Analysis of the Factors Controlling Stereoselectivity. The Journal of Organic Chemistry 71:14, pages 5171-5178.
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José Barluenga, María Marco‐Arias, Francisco González‐Bobes, Alfredo Ballesteros & José M. González. (2004) Reaction of Alkenes with Hydrogen Peroxide and Sodium Iodide: A Nonenzymatic Biogenic‐Like Approach to Iodohydrins. Chemistry – A European Journal 10:7, pages 1677-1682.
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Alain Bekaert, Olivier Barberan, Marina Gervais & Jean-Daniel Brion. (2000) Direct α-iodination of ketones using iodine/SeO2. Tetrahedron Letters 41:16, pages 2903-2905.
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. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 1103 1295 .
Peter L. Spargo. 1995. Comprehensive Organic Functional Group Transformations. Comprehensive Organic Functional Group Transformations 1 36 .
Sigeru Torii & Tsutomu Inokuchi. 1991. Comprehensive Organic Synthesis. Comprehensive Organic Synthesis 527 540 .
J.M. Aizpurua, M. Juaristi, B. Lecea & C. Palomo. (1985) Reagents and synthetic methods—40. Tetrahedron 41:14, pages 2903-2911.
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Yashwant D. Vankar & G. Kumaravel. (1984) N-chlorosuccinimide/sodium iodide: A convenient source of N-iodosuccinimide. Synthesis of α-iodo carbonyl compounds and trans-1,2-iodoacetates. Tetrahedron Letters 25:2, pages 233-236.
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M. D'AURIA, F. D'ONOFRIO, G. PIANCATELLI & A. SCETTRI. (2016) ChemInform Abstract: STUDIES ON REACTIVITY OF PYRIDINIUM CHLOROCHROMATE‐IODINE SYSTEM: AN EFFICIENT METHOD FOR CONVERTING ENOL SILYL ETHERS INTO α‐IODO KETONES. Chemischer Informationsdienst 14:33.
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