Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5219068 | Tetrahedron | 2012 | 5 Pages |
Abstract
The asymmetric epoxidation of styrene derivatives by H2O2 (or UHP) to give optically active epoxides (ee up to 81%) and hydroxylation of alkanes to give optically active secondary alcohols (ee up to 78%) were carried out in methanol and water using chiral water-soluble iron porphyrins as catalysts.
Graphical abstractDownload full-size imageThe asymmetric epoxidation of styrene derivatives by H2O2 (or UHP) to give optically active epoxides (ee up to 81%) and hydroxylation of alkanes to give optically active secondary alcohols (ee up to 78%) were carried out in methanol and water using chiral water-soluble iron porphyrins as catalysts.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Paul Le Maux, Hassan F. Srour, Gérard Simonneaux,