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  • Highly efficient isobutyraldehyde-mediated epoxidation of cyclic alkenes with dioxygen catalyzed by a novel dimeric manganese(II) complex containing an easy-to-prepare flexible carboxamide ligand.

Highly efficient isobutyraldehyde-mediated epoxidation of cyclic alkenes with dioxygen catalyzed by a novel dimeric manganese(II) complex containing an easy-to-prepare flexible carboxamide ligand.

Inorganic chemistry (2009-05-28)
Hamid Reza Khavasi, Koroush Sasan, Mahtab Pirouzmand, Samad Nejad Ebrahimi
ZUSAMMENFASSUNG

Dioxygen epoxidation of cyclic alkenes into their corresponding epoxides was successfully achieved in good yield by using a novel binuclear manganese carboxamide complex as the catalyst and isobutyraldehyde as the cosubstrate.

MATERIALIEN
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Produktbeschreibung

Sigma-Aldrich
Isobutyraldehyd, ≥99%
Sigma-Aldrich
Isobutyraldehyd, ≥98%, FG
Sigma-Aldrich
Isobutyraldehyd, dry, 98%
Sigma-Aldrich
Isobutyraldehyd, natural, 96%, FG
Sigma-Aldrich
Isobutyraldehyd, 98%
Sigma-Aldrich
Isobutyraldehyd, redistilled, ≥99.5%