Epoxidation of ethene: a new substituent twist.
DOI: 10.14469/hpc/4909 Metadata
Created: 2018-12-21 08:51
Last modified: 2018-12-21 08:52
License: Creative Commons: Public Domain Dedication 1.0
Funding: (none given)
Description
Five years back, I speculated about the mechanism of the epoxidation of ethene by a peracid, concluding that kinetic isotope effects provided interesting evidence that this mechanism is highly asynchronous and involves a so-called  "hidden intermediate".  Here  I revisit this reaction in which a small change is applied to the atoms involved.
Member of collection / collaboration
| DOI | Description |
|---|---|
| 10.14469/hpc/177 | Computation data for Henry Rzepa's blog |
Members
| DOI | Description |
|---|---|
| 10.14469/hpc/4786 | Ethanimidoperoxoic acid epoxidation of propene |