Modular access to vicinally functionalized allylic (thio)morpholinonates and piperidinonates by substrate-controlled annulation of 1,3-azadienes with hexacyclic anhydrides

A modular substrate-controlled hexannulation of inherently promiscuous 1,3-azadienes with hexacyclic anhydrides, which affords versatile vicinally functionalized allylic lactams, in high yields, regio- and stereoselectivities is described. A modular substrate-controlled hexannulation of 1,3-azadiene...

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Veröffentlicht in:Organic & biomolecular chemistry 2016-09, Vol.14 (37), p.8864-8872
Hauptverfasser: Braunstein, Hannah, Langevin, Spencer, Khim, Monique, Adamson, Jonathan, Hovenkotter, Katie, Kotlarz, Lindsey, Mansker, Brandon, Beng, Timothy K
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Sprache:eng
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Zusammenfassung:A modular substrate-controlled hexannulation of inherently promiscuous 1,3-azadienes with hexacyclic anhydrides, which affords versatile vicinally functionalized allylic lactams, in high yields, regio- and stereoselectivities is described. A modular substrate-controlled hexannulation of 1,3-azadienes with hexacyclic anhydrides, which affords versatile vicinally functionalized allylic lactams, in high yields, regio- and stereoselectivities is described.
ISSN:1477-0520
1477-0539
DOI:10.1039/c6ob01526c