Ring-expansion of tertiary cyclic alpha-vinylamines by tandem conjugate addition to (p-toluenesulfonyl)ethyne and formal 3-aza-Cope rearrangement

A novel ring-expansion protocol is based on the conjugate additions of cyclic alpha-vinylamines to (p-toluenesulfonyl)ethyne, followed by aza-Cope rearrangements of the resulting zwitterions, to afford medium and large-ring cyclic amines under remarkably mild conditions.

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2006-01 (37), p.3903-3905
Hauptverfasser: Weston, Mitchell H, Nakajima, Katsumasa, Parvez, Masood, Back, Thomas G
Format: Artikel
Sprache:eng
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Zusammenfassung:A novel ring-expansion protocol is based on the conjugate additions of cyclic alpha-vinylamines to (p-toluenesulfonyl)ethyne, followed by aza-Cope rearrangements of the resulting zwitterions, to afford medium and large-ring cyclic amines under remarkably mild conditions.
ISSN:1359-7345
1364-548X
DOI:10.1039/b607713g