Starting from easily available (+)-norcamphor and according to an established approach, the 2-benzo[b]furyl hydroperoxide exo-5 was obtained in 58% overall yield. In order to ascertain the impact of the modification on the activity of this chiral oxidant, a study was carried out employing it in the asymmetric epoxidation of an allylic alcohol and alpha,beta-enones.

Synthesis of a benzo[b]furyl (+)-Norcamphor-derived hydroperoxide: study of the activity as an oxidant in asymmetric epoxidations

LATTANZI, Alessandra;SCETTRI, Arrigo
2008-01-01

Abstract

Starting from easily available (+)-norcamphor and according to an established approach, the 2-benzo[b]furyl hydroperoxide exo-5 was obtained in 58% overall yield. In order to ascertain the impact of the modification on the activity of this chiral oxidant, a study was carried out employing it in the asymmetric epoxidation of an allylic alcohol and alpha,beta-enones.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11386/1850678
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