Palladium-catalyzed asymmetric annulation between aryl iodides and racemic epoxides using a chiral norbornene cocatalyst

Herein, we describe our initial development of an asymmetric Pd-catalyzed annulation between aryl iodides and racemic epoxides for synthesis of 2,3-dihydrobenzofurans using a chiral norbornene cocatalyst. A series of enantiopure ester-, amide- and imide-substituted norbornenes have been prepared wit...

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Veröffentlicht in:Organic Chemistry Frontiers 2018-11, Vol.5 (21), p.3108-3112
Hauptverfasser: Li, Renhe, Liu, Feipeng, Dong, Guangbin
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Sprache:eng
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Zusammenfassung:Herein, we describe our initial development of an asymmetric Pd-catalyzed annulation between aryl iodides and racemic epoxides for synthesis of 2,3-dihydrobenzofurans using a chiral norbornene cocatalyst. A series of enantiopure ester-, amide- and imide-substituted norbornenes have been prepared with a reliable synthetic route. Promising enantioselectivity (42–45% ee) has been observed using the isopropyl ester-substituted norbornene ( N1* ) and the amide-substituted norbornene ( N7* ).
ISSN:2052-4129
2052-4110
2052-4129
2052-4110
DOI:10.1039/c8qo00808f