Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5219173 | Tetrahedron | 2012 | 7 Pages |
Abstract
Concise and efficient four-component tandem approaches to polysubstituted indolizines have been developed under metal-free and mild aerobic conditions in refluxing acetonitrile. The mechanism of the novel reactions was proposed involving the formation of pyridinium ylides and α,β-unsaturated ketones with subsequent 1,3-dipolar cycloaddition and aromatization reaction.
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