Synlett, Table of Contents ACCOUNT© Georg Thieme Verlag Stuttgart · New YorkSynthetic Use of Molecular Iodine for Organic SynthesisHideo Togo*, Shinpei IidaGraduate School of Science and Technology, Chiba University, Yayoi-cho 1-33, Inage-ku, Chiba 263-8522 Japane-Mail: togo@faculty.chiba-u.jp; Recommend Article Abstract Buy Article All articles of this category Abstract The synthetic use of molecular iodine is described. Iodine is a universal oxidizing agent, especially for the oxidation of alcohols and aldehydes to esters, nitriles and amides. Further applications are the introduction of protecting groups, deprotection, iodocyclization, C-C bond formation, and formation of heterocycles. 1 Introduction 2 Oxidation of Alcohols and Aldehydes to Esters, Nitriles, Amides 3 Oxidation of Sulfides 4 Oxidation to Aromatics 5 Introduction of Protecting Groups 6 Deprotection 7 Iodocyclization 8 C-C Bond Formation 9 Formation of Heterocycles 10 Others Key words iodine - oxidation - protection - deprotection - iodocyclization - heterocycles Full Text References References <A NAME="RA41306ST-1A">1a</A> Lieben A. Ann. 1870, 7: 218 <A NAME="RA41306ST-1B">1b</A> Org. Synth., Coll. Vol. II Springer; Berlin: 1966. p.428 <A NAME="RA41306ST-2">2</A> Cruickshank FR. Benson SW. J. Phys. Chem. 1969, 73: 733 <A NAME="RA41306ST-3A">3a</A> Inch TD. Ley RV. Rich P. J. Chem. Soc. C 1968, 1693 <A NAME="RA41306ST-3B">3b</A> Yamada S. Morizono D. Yamamoto K. Tetrahedron Lett. 1992, 33: 4329 <A NAME="RA41306ST-3C">3c</A> Yamamoto K. Shimizu M. Yamada S. J. 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