Enantioselective Organocatalyzed Michael Additions of Nitroalkanes to 4-Arylidenedihydrofuran-2,3-diones and 4-Arylidenepyrrolidine-2,3-diones - Aix-Marseille Université Access content directly
Journal Articles European Journal of Organic Chemistry Year : 2020

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

Abstract

Despite tremendous efforts towards the development of organocatalytic enantioselective Michael additions of nitroalkanes to α,β‐unsaturated carbonyl compounds, highly substituted electrophiles remain challenging. β‐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.
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Dates and versions

hal-03163964 , version 1 (09-03-2021)

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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⟩

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