Image (Illustration) Année : 2020

Enantioselective Organocatalyzed Michael Additions of Nitroalkanes to 4-Arylidenedihydrofuran-2,3-diones and 4-Arylidenepyrrolidine-2,3-diones

Résumé

Tremendous efforts have been devoted to the development of organocatalytic enantioselective Michael additions of nitroalkanes to α,-unsaturated carbonyl compounds. However, using highly substituted electrophiles remain challenging, since the additional substituents decrease the electrophilicity. -Arylidene-α-ketolactones and α-ketolactams are used as highly electrophilic Michael acceptors that afford the corresponding products in moderate to good yields, with high enantioselectivities. This success relies on their rigid structure that prevents deconjugation and the efficient recognition of the α-dicarbonyl motif by the hydrogen-bond donor catalyst.

Domaines

HAL

Décrit hal-03163964 Article Mouhamadou Fofana, Yohan Dudognon, Laura Bertrand, Thierry Constantieux, Jean Rodriguez, et al.. Enantioselective Organocatalyzed Michael Additions of Nitroalkanes to 4-Arylidenedihydrofuran-2,3-diones and 4-Arylidenepyrrolidine-2,3-diones. European Journal of Organic Chemistry, 2020, 2020 (23), pp.3486-3490. ⟨10.1002/ejoc.202000460⟩. ⟨hal-03163964⟩

Dates et versions

hal-03163974 , version 1 (09-03-2021)

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Identifiants

  • HAL Id : hal-03163974 , version 1

Citer

Mouhamadou Fofana, Yohan Dudognon, Laura Bertrand, Thierry Constantieux, Jean Rodriguez, et al.. Enantioselective Organocatalyzed Michael Additions of Nitroalkanes to 4-Arylidenedihydrofuran-2,3-diones and 4-Arylidenepyrrolidine-2,3-diones. Illustration. France. 2020. ⟨hal-03163974⟩
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