The Mechanism of the Acid-Catalyzed Ring Opening of Epoxides - A Reinterpretative Review
Summarizing all available evidence we may conclude that the acid-catalyzed ring opening of primary and secondary epoxides proceeds with Walden inversion by a SN2 (or overall A-2) mechanism. A fractional positive charge at the reacting carbon atom may be postulated without taking recourse to the “bo...
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| Main Author: | |
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| Format: | Article |
| Language: | deu |
| Published: |
Swiss Chemical Society
1974-01-01
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| Series: | CHIMIA |
| Online Access: | https://www.chimia.ch/chimia/article/view/9115 |
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