Enantiomerically enriched (3-furyl)-2-pyran derivatives, key-intermediates in the synthesis of the pharmacophoric pyranofuranone system of the bioactive natural products manoalide and cacospongionolide B, are easily accessible by a rapid sequence involving a chiral allylation and a ring closing metathesis reaction

A three-step and enantioselective synthesis of (−)-(S)- or (+)-(R)-2-(furan-3-yl)-3,6-dihydro-2H-pyrans

DE ROSA, Margherita;SCETTRI, Arrigo
2000

Abstract

Enantiomerically enriched (3-furyl)-2-pyran derivatives, key-intermediates in the synthesis of the pharmacophoric pyranofuranone system of the bioactive natural products manoalide and cacospongionolide B, are easily accessible by a rapid sequence involving a chiral allylation and a ring closing metathesis reaction
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11386/3003482
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