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In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen. This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers.
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epoxides ethylene oxide reaction oxygen ring epoxy alkene epoxidation catalysts reactions also propylene group used mechanism alkenes give one oxidation
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Epoxide | is a | cyclic ether | 0.90 | text |
| peroxides | instance of | such as enones and acryl derivatives can be epoxidized using nucleophilic oxygen compounds | 0.80 | text |
| mCPBA | instance of | This approach involves the oxidation of the alkene with a peroxyacid | 0.80 | text |
| Epoxide | related to Asymmetric epoxidations | Chiral | 0.60 | section |
| Epoxide | related to Asymmetric epoxidations | When | 0.60 | section |
| Epoxide | related to Asymmetric epoxidations | Prominent | 0.60 | section |
| Epoxide | related to Asymmetric epoxidations | Sharpless | 0.60 | section |
| Epoxide | related to Asymmetric epoxidations | Jacobsen | 0.60 | section |
| Epoxide | related to Asymmetric epoxidations | Shi | 0.60 | section |
| Epoxide | related to Biosynthesis | Epoxides | 0.60 | section |
| Epoxide | related to Biosynthesis | They | 0.60 | section |
| Epoxide | related to Biosynthesis | P450 | 0.60 | section |
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