## Abstract Umsetzung von 4‐Methyl‐1,4‐cyclohexadien‐1‐carbonsäure‐methylester (**(2)** mit Methyllithium führt zum tertiären Alkohol **3**, der zum Vinyläther **4** umgesetzt wird. __Claisen__‐Umlagerung von **4** gibt den Aldehyd **5**, der mit CH~3~MgJ zum sekundären Alkohol **6** reagiert. Oxid
✦ LIBER ✦
Synthesis of 6-Methyl-4-(1-methyl-2-buten-1-yl)-2-(2-cyclohexen-1-yl)- and 6-Methyl-4-(1-methyl-2-buten-1-yl)-2-(1-cyclohexen-1-yl)anilines
✍ Scribed by R. R. Gataullin; R. R. Ishberdina; A. M. Sotnikov; I. B. Abdrakhmanov
- Publisher
- SP MAIK Nauka/Interperiodica
- Year
- 2005
- Tongue
- English
- Weight
- 47 KB
- Volume
- 78
- Category
- Article
- ISSN
- 1070-4272
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