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Synthesis of Functionalized Monoaryl-λ3-iodanes through Chemo- and Site-Selective ipso-Substitution Reactions
Authors:Narumi Komami  Keitaro Matsuoka  Ayako Nakano  Dr Masahiro Kojima  Dr Tatsuhiko Yoshino  Prof Dr Shigeki Matsunaga
Institution:1. Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-ku, Sapporo, 060-0812 Japan

These authors contributed equally to this work.;2. Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-ku, Sapporo, 060-0812 Japan

Abstract:Monoaryl-λ3-iodanes are potentially attractive arylating agents. They are generally synthesized from aryl iodides via oxidation, which can cause functional group incompatibility, especially when polyfunctionalized derivatives are desired. This work describes the direct synthesis of monoaryl-λ3-iodanes through a chemoselective ipso-substitution reaction of arylgermanes and arylstannanes with iodine tris(trifluoroacetate). The generated iodanes were converted to iodonium ylides or used for further transformations in one pot. The presented method enables the preparation of polyfunctionalized monoaryl-λ3-iodanes.
Keywords:arylation  germanium  hypervalent iodine  iodonium ylide  ipso-substitution
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