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Tandem Cyclization of a Bispyridinium Chloride: Facile Synthesis of Substituted Indolizines

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2013

Year

Abstract

Functionalized indolizines were prepared by a one-pot cascade reaction from bispyridinium salts. This mild experimental procedure allowed the isolation of the product in very good yield. Combination of the indolizine derivative with electrophiles confirmed the reactivity of the C<sub>3</sub> ring carbon and allowed the bromination, formylation, hydroxymethylation, and dimerization of the indolizine scaffold.