1344715-68-9Relevant academic research and scientific papers
Conjugate addition of 1,3-dicarbonyl compounds to maleimides using a chiral C2-symmetric bis(2-aminobenzimidazole) as recyclable organocatalyst
Gomez-Torres, Eduardo,Alonso, Diego A.,Gomez-Bengoa, Enrique,Najera, Carmen
, p. 6106 - 6109 (2011)
The recyclable chiral 2-aminobenzimidazole-derived organocatalyst 1f efficiently promotes the room temperature asymmetric conjugate addition of 1,3-diketones, β-ketoesters, and malonates to maleimide and N-substituted maleimides, affording the correspondi
Enantioselective synthesis of succinimides by michael addition of 1,3-dicarbonyl compounds to maleimides catalyzed by a chiral bis(2-aminobenzimidazole) organocatalyst
Gomez-Torres, Eduardo,Alonso, Diego A.,Gomez-Bengoa, Enrique,Najera, Carmen
supporting information, p. 1434 - 1440 (2013/04/23)
A wide variety of chiral succinimides have been prepared in high yields and enantioselectivities by asymmetric conjugate addition of 1,3-dicarbonyl compounds to maleimides under very mild reaction conditions using a bifunctional benzimidazole-derived orga
