A strategy for the preparation of a supported ‘salen-type’ Mn(III) catalyst derived from d-glucose is described. The compound has been prepared by introducing the ligand functions at positions 2 and 3 of the sugar, which has been subsequently anchored to a CHO-modified Wang resin through formation of a 4,6-O-benzylidene ring. The activity of the catalyst in the asymmetric epoxidation of styrenes has been investigated by using four different oxidants.

A supported Mn(III) catalyst based on D-glucose in the asymmetric epoxidation of styrenes / Borriello, Carmela; DEL LITTO, Raffaella; Panunzi, Achille; Ruffo, Francesco. - In: INORGANIC CHEMISTRY COMMUNICATIONS. - ISSN 1387-7003. - STAMPA. - 8:8(2005), pp. 717-721. [10.1016/j.inoche.2005.04.017]

A supported Mn(III) catalyst based on D-glucose in the asymmetric epoxidation of styrenes

BORRIELLO, CARMELA;DEL LITTO, Raffaella;PANUNZI, ACHILLE;RUFFO, FRANCESCO
2005

Abstract

A strategy for the preparation of a supported ‘salen-type’ Mn(III) catalyst derived from d-glucose is described. The compound has been prepared by introducing the ligand functions at positions 2 and 3 of the sugar, which has been subsequently anchored to a CHO-modified Wang resin through formation of a 4,6-O-benzylidene ring. The activity of the catalyst in the asymmetric epoxidation of styrenes has been investigated by using four different oxidants.
2005
A supported Mn(III) catalyst based on D-glucose in the asymmetric epoxidation of styrenes / Borriello, Carmela; DEL LITTO, Raffaella; Panunzi, Achille; Ruffo, Francesco. - In: INORGANIC CHEMISTRY COMMUNICATIONS. - ISSN 1387-7003. - STAMPA. - 8:8(2005), pp. 717-721. [10.1016/j.inoche.2005.04.017]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/309686
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