Abstract
A series of sterically hindered manganese porphyrins are shown to be shape-selective catalysts for the epoxidation of a variety of dienes; product ration differences for conjugated vs. non-conjugated dienes indicate the existence of at least two competing epoxidation pathways.
Original language | English (US) |
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Pages (from-to) | 200-202 |
Number of pages | 3 |
Journal | Journal of the Chemical Society, Chemical Communications |
Issue number | 3 |
DOIs | |
State | Published - 1987 |
ASJC Scopus subject areas
- Molecular Medicine