The palladium-catalyzed reaction of (hetero)aryl bromides, chlorides, and nonaflates with α-allyl-β-ketoesters provides ready efficient access to functionalized 2,3-dihydrofurans. The reaction tolerates several useful substituents including chloro, fluoro, ether, ketone, ester, cyano, and nitro groups. © The Royal Society of Chemistry 2011.

Functionalized 2,3-dihydrofurans via palladium-catalyzed oxyarylation of α-allyl-β-ketoesters / Cacchi, Sandro; Fabrizi, Giancarlo; Goggiamani, Antonella; Iazzetti, Antonia; David, Madec; Giovanni, Poli; Guillaume, Prestat. - In: ORGANIC & BIOMOLECULAR CHEMISTRY. - ISSN 1477-0520. - STAMPA. - 9:24(2011), pp. 8233-8236. [10.1039/c1ob06593a]

Functionalized 2,3-dihydrofurans via palladium-catalyzed oxyarylation of α-allyl-β-ketoesters

CACCHI, Sandro;FABRIZI, Giancarlo;GOGGIAMANI, ANTONELLA;IAZZETTI, Antonia;
2011

Abstract

The palladium-catalyzed reaction of (hetero)aryl bromides, chlorides, and nonaflates with α-allyl-β-ketoesters provides ready efficient access to functionalized 2,3-dihydrofurans. The reaction tolerates several useful substituents including chloro, fluoro, ether, ketone, ester, cyano, and nitro groups. © The Royal Society of Chemistry 2011.
01 Pubblicazione su rivista::01a Articolo in rivista
Functionalized 2,3-dihydrofurans via palladium-catalyzed oxyarylation of α-allyl-β-ketoesters / Cacchi, Sandro; Fabrizi, Giancarlo; Goggiamani, Antonella; Iazzetti, Antonia; David, Madec; Giovanni, Poli; Guillaume, Prestat. - In: ORGANIC & BIOMOLECULAR CHEMISTRY. - ISSN 1477-0520. - STAMPA. - 9:24(2011), pp. 8233-8236. [10.1039/c1ob06593a]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/433689
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