2018•HeterocyclesOpen access

Metal-Free Oxidative Cross-Coupling of Pyrroles with Electron-Rich Arenes Using Recyclable Hypervalent Iodine(III) Reagent

Yasuyuki Kita, Koji Morimoto, Tohru Kamitanaka, Toshifumi Dohi

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Abstract

The facile and clean oxidative cross-coupling reaction of pyrroles has been developed using the recyclable hypervalent iodine(III) reagents having an adamantane core.The recyclable iodine(III) reagent could be recovered from the reaction mixtures as the corresponding reduced forms, i.e., the tetraiodide 2, by a simple solid-liquid separation.By re-oxidizing the recovered 2 to the initial reagent 1a using m-chloroperbenzoic acid (mCPBA), the reagent 1a can be reused.

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The facile and clean oxidative cross-coupling reaction of pyrroles has been developed using the recyclable hypervalent iodine(III) reagents having an adamantane core.The recyclable iodine(III) reagent could be recovered from the reaction mixtures as the corresponding reduced forms, i.e., the tetraiodide 2, by a simple solid-liquid separation.By re-oxidizing the recovered 2 to the initial reagent 1a using m-chloroperbenzoic acid (mCPBA), the reagent 1a can be reused.

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Available abstract

The facile and clean oxidative cross-coupling reaction of pyrroles has been developed using the recyclable hypervalent iodine(III) reagents having an adamantane core.The recyclable iodine(III) reagent could be recovered from the reaction mixtures as the corresponding reduced forms, i.e., the tetraiodide 2, by a simple solid-liquid separation.By re-oxidizing the recovered 2 to the initial reagent 1a using m-chloroperbenzoic acid (mCPBA), the reagent 1a can be reused.

Key concepts: Hypervalent molecule, Reagent, Chemistry, Oxidizing agent, Iodine, Metal, Oxidative coupling of methane, Organic chemistry

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