Two novel chiral C2-symmetrical ferrocenyl 'salen-type' ligands were prepared via reaction of suitable ferrocenyldiamines with 3,5-di-tert-butylsalicylaldehyde and tested in the asymmetric epoxidation of unfunctionalized alkenes. Although the asymmetric induction was quite low, an unusually high trans/cis-epoxide ratio and high reactivity of a trans-alkene substrate were observed.

Synthesis of novel chiral 'salen-type' ferrocenyl ligands

Patti A;Pedotti S;
2007

Abstract

Two novel chiral C2-symmetrical ferrocenyl 'salen-type' ligands were prepared via reaction of suitable ferrocenyldiamines with 3,5-di-tert-butylsalicylaldehyde and tested in the asymmetric epoxidation of unfunctionalized alkenes. Although the asymmetric induction was quite low, an unusually high trans/cis-epoxide ratio and high reactivity of a trans-alkene substrate were observed.
2007
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/157302
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