Regioselective Synthesis of α-erfluoroalkylated Ketals via Double Michael Addition of Alcohols to Activated Alkynes - Aix-Marseille Université Accéder directement au contenu
Article Dans Une Revue Synthesis: Journal of Synthetic Organic Chemistry Année : 2015

Regioselective Synthesis of α-erfluoroalkylated Ketals via Double Michael Addition of Alcohols to Activated Alkynes

Résumé

An efficient method was developed for the synthesis of alkyl 3,3-dialkoxy-3-(perfluoroalkyl)propanoates from ethyl 3-(perfluoroalkyl)propynoates and alcohols using a base-catalyzed double Michael addition reaction (which was accompanied by transesterification in the case of MeOH, EtOH, PrOH, and BuOH). This method provides easy access to the product α-perfluoroalkyl ketals with reasonable to good yields with total regioselectivity. This procedure does not require the use of expensive supplementary additives for the preparation of α-perfluoroalkyl ketals which are very sensitive to acidic conditions.
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Dates et versions

hal-02633788 , version 1 (27-05-2020)

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Guy Judicaël Ella Ndong, Jean-Luc Parrain, Mohamed Abarbri. Regioselective Synthesis of α-erfluoroalkylated Ketals via Double Michael Addition of Alcohols to Activated Alkynes. Synthesis: Journal of Synthetic Organic Chemistry, 2015, 47 (17), pp.2635-2640. ⟨10.1055/s-0034-1380753⟩. ⟨hal-02633788⟩
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