α-Ethoxybutenyltributyletains precurseurs d'α-ethoxybutenyllithiums: Application a la synthese d'enones via les monoethers homoallyliques d'α-glycols
JP Quintard, B Elissondo, T Hattich…
Index: Quintard, Jean-Paul; Elissondo, Bernard; Hattich, Thomas; Pereyre, Michel Journal of Organometallic Chemistry, 1985 , vol. 285, p. 149 - 162
Full Text: HTML
Citation Number: 9
Abstract
Upon transmetallation (BuLi/THF/− 70°C), these new reagents afford α-ethoxybutenyllithiums, which when treated at − 70°C with allyl halides or carbonyl compounds give dihomoallyl ethers or homoallyl monoethers of α-glycols. The latter compounds upon acidic treatment afford α,β- or β,γ-enones, depending on the structure of the substrate and on the experimental conditions. ... Les α-éthoxybutényltributylétains sont aisément synthétisés par réaction ...
Related Articles:
[Duchene, Alain; Quintard, Jean-Paul Journal of the Chemical Society, Chemical Communications, 1987 , # 1 p. 29 - 30]