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A simple, two-step synthesis of 3-iodoindoles
Authors:Muhammad Amjad
Institution:Cardiff School of Chemistry, Cardiff University, PO Box 912, Cardiff CF10 3TB, UK
Abstract:2-Halo-anilines, protected as the corresponding sulfonamides or carbamates, can be converted very efficiently into 3-iodoindoles by sequential Sonogashira coupling with a 1-alkyne and 5-endo-dig iodocyclisation. Azaindoles can also be obtained using this methodology.
Keywords:5-Endo-dig  Iodocyclisation  Sonogashira  Indole  Synthesis
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