Free Radical-Mediated Vinyl Amination:  Access to N,N-Dialkyl Enamines and Their β-Stannyl and β-Thio Derivatives

The first examples of free radical-mediated vinyl amination are described by nonconventional vinyl radical addition to azomethine nitrogen. This new vinyl amination protocol is mild and provides convenient synthetic access to nonstabilized N,N-dialkyl enamines and tandem bond-forming processes.

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Veröffentlicht in:Organic letters 2002-11, Vol.4 (24), p.4197-4200
Hauptverfasser: Prabhakaran, Erode N, Nugent, Benjamin M, Williams, Amie L, Nailor, Kristen E, Johnston, Jeffrey N
Format: Artikel
Sprache:eng
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Zusammenfassung:The first examples of free radical-mediated vinyl amination are described by nonconventional vinyl radical addition to azomethine nitrogen. This new vinyl amination protocol is mild and provides convenient synthetic access to nonstabilized N,N-dialkyl enamines and tandem bond-forming processes.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol027064u