Cyclic Sulfamidates as Vehicles for the Synthesis of Substituted Lactams
A structurally diverse series of mono- and disubstituted 1,2- and 1,3-cyclic sulfamidates react with stabilized enolates, including malonate and phosphonoacetate variants, to provide, after lactamization, substituted and α-functionalized pyrrolidinone and piperidinone derivatives.
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Veröffentlicht in: | Organic letters 2004-12, Vol.6 (25), p.4727-4730 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A structurally diverse series of mono- and disubstituted 1,2- and 1,3-cyclic sulfamidates react with stabilized enolates, including malonate and phosphonoacetate variants, to provide, after lactamization, substituted and α-functionalized pyrrolidinone and piperidinone derivatives. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/ol048036+ |