Article Dans Une Revue SYNLETT Année : 2018

Weinreb β-Ketoamides in Enantioselective Organocatalysis: A Balance between Reactivity and Selectivity

Résumé

β-Dicarbonyl compounds have established themselves as substrates of choice in enantioselective organocatalysis because of their easy activation. Among them, β-diketones, β-diesters and β-ketoesters lead the dance and there has been only limited work with other β-dicarbonyl compounds as pronucleophiles. In this Synpacts article, we wish to discuss our recent contributions to the introduction of Weinreb β-ketoamides in organocatalyzed transformations, where they can provide an interesting balance between reactivity and selectivity, with also interesting potentialities in terms of post-functionalization.

Fichier principal
Vignette du fichier
Pub_XB_1bis.pdf (3.55 Mo) Télécharger le fichier
Origine Fichiers produits par l'(les) auteur(s)
Licence
Loading...
HAL

Est décrite par medihal-01723131 Image Haiying Du, Yohan Dudognon, Jean Rodriguez, Thierry Constantieux, Xavier Bugaut. Weinreb β-Ketoamides in Enantioselective Organocatalysis: A Balance between Reactivity and Selectivity. Illustration. France. 2017. ⟨medihal-01723131⟩

Dates et versions

hal-01723120 , version 1 (05-03-2018)

Licence

Identifiants

Citer

Haiying Du, Yohan Dudognon, Jean Rodriguez, Thierry Constantieux, Xavier Bugaut. Weinreb β-Ketoamides in Enantioselective Organocatalysis: A Balance between Reactivity and Selectivity. SYNLETT, In press, ⟨10.1055/s-0036-1591870⟩. ⟨hal-01723120⟩
166 Consultations
381 Téléchargements

Altmetric

Partager

  • More