| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274059 | Tetrahedron Letters | 2009 | 5 Pages |
Abstract
Ti(III)-mediated radical cyclization of β-aminoacrylate containing 2,3-epoxy alcohol moieties led to the formation of highly substituted piperidine and pyrrolidine rings. The pyrrolidine ring system was then transformed into an indolizidine framework present in many natural products.
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