1148116-72-6Relevant articles and documents
Asymmetric Michael reaction of aldehydes with β-nitroalkenes catalyzed by pyrrolidine-camphor derived organocatalysts bearing hydrogen-bond donors
Weng, Jiang,Ai, Hui-Bing,Luo, Ren-Shi,Lu, Gui
, p. 271 - 275 (2012)
Several pyrrolidine-camphor derived organocatalysts were designed and synthesized. These organocatalysts were used for direct Michael reaction of aldehydes with nitroalkenes to give the desired γ-nitrocarbonyl compounds in high yields (up to 99%), high di
Conformational Control of Tetrahydropyran-Based Hybrid Dipeptide Catalysts Improves Activity and Stereoselectivity
Borges-González, Jorge,García-Monzón, Irma,Martín, Tomás
supporting information, p. 2141 - 2147 (2019/03/23)
Herein, we introduce and demonstrate how carbohydrates can be used as conformational control units of organocatalysts to tune their catalytic properties. New hybrid dipeptide-like organocatalysts based on ζ-sugar aminoacids and proline were prepared and t
Tetrahydropyran-Based Hybrid Dipeptides as Asymmetric Catalysts for Michael Addition of Aldehydes to β-Nitrostyrenes
Borges-González, Jorge,Feher-Voelger, Andrés,Crisóstomo, Fernando Pinacho,Morales, Ezequiel Q.,Martín, Tomás
supporting information, p. 576 - 583 (2017/02/23)
A new series of hybrid dipeptide-like organocatalysts based on pyranoid ?- or ζ-amino acids and proline have been prepared for the asymmetric Michael addition of aldehydes to β-nitrostyrenes. The reaction proceeds under mild conditions to afford a wide ra