3-Metallierte Enamine als Homoenolate – Eine neue Entwicklung in der Enaminchemie
The deprotonation of tertiary enamines at C-3 is described. The resulting highly nucleophilic 1-aminoallylic anions 8 react with a large number of electrophiles at C-3 to form homologated enamines 10 (γ-products). By this reaction enamines, normally considered as substitutes for enolates 3 can be u...
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| Format: | Article |
| Language: | deu |
| Published: |
Swiss Chemical Society
1977-10-01
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| Series: | CHIMIA |
| Online Access: | https://www.chimia.ch/chimia/article/view/9382 |
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