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In organic chemistry, an imine (/ɪˈmiːn/ or /ˈɪmɪn/) is a functional group or organic compound containing a carbon–nitrogen double bond (.mw-parser-output .template-chem2-su{display:inline-block;font-size:80%;line-height:1;vertical-align:-0.35em}.mw-parser-output .template-chem2-su>span{display:block;text-align:left}.mw-parser-output…
Synthesis of imines, Reactions & Nomenclature and classification
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imines reaction amines primary aldehydes synthesis reactions carbon nitrogen ketones compound compounds derived organic group atom amine polyimines secondary schiff
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Imine | is a | Amadori rearrangement.A methylene transfer reaction of an imine by an unstabilised sulphonium ylide can give an aziridine system | 0.90 | text |
| Tris | instance of | several reagents | 0.80 | text |
| Imine | has method | Several | 0.60 | section |
| Imine | has method | Reaction | 0.60 | section |
| Imine | has method | The | 0.60 | section |
| Imine | has method | Wittig | 0.60 | section |
| Imine | has method | Condensation | 0.60 | section |
| Imine | has method | N-haloamines | 0.60 | section |
| Imine | has method | Stieglitz | 0.60 | section |
| Imine | has method | By | 0.60 | section |
| Imine | has method | Schmidt | 0.60 | section |
| Imine | has method | Hoesch | 0.60 | section |
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