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Three-component strategy toward 5-membered heterocycles from isocyanide dibromides.

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Abstract

A three-component strategy starting from isocyanides allows a straightforward synthesis of five-membered ring heterocycles. New cascades were developed involving the addition of a nitrogenated nucleophile-an azide or a tetrazole-on isocyanide dibromides, an electrocyclization, and a Suzuki coupling, which afford new accesses to tetrazole and triazole scaffolds.(Figure Presented)

Original languageEnglish
Pages (from-to)1261-1263
Number of pages3
JournalOrganic Letters
Volume13
Issue number5
DOIs
Publication statusPublished - 4 Mar 2011
Externally publishedYes

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