A Transition Metal Catalyzed Reaction of Aromatic Acyl Chlorides with Epoxides
In a transition metal catalyzed reaction of aroyl chlorides with epoxides a change from palladium to ruthenium brings about a change in regioselectivity. A participation of the transition metal in the ring opening step is now evident.
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| Format: | Article |
| Language: | deu |
| Published: |
Swiss Chemical Society
1985-12-01
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| Series: | CHIMIA |
| Online Access: | https://www.chimia.ch/chimia/article/view/9703 |
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