Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5279448 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
α,β-Unsaturated sulfinylimines derived from α-amino acids undergo aza-Diels-Alder reaction with electron rich dienophiles such as enolethers and enamines. Subsequent elimination of sulfinyl and amine or alkoxy moiety on the resulting cycloadducts affords pyridines derived from α-amino acids.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Francisco Palacios, Javier Vicario, Domitila Aparicio,