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Diastereoselective auxiliary- and catalyst-controlled intramolecular aza-Michael reaction for the elaboration of enantioenriched 3-substituted isoindolinones. Application to the synthesis of a new pazinaclone analogue

A new asymmetric organocatalyzed intramolecular aza-Michael reaction by means of both a chiral auxiliary and a catalyst for stereocontrol is reported for the synthesis of optically active isoindolinones. A selected cinchoninium salt was used as phase-transfer catalyst in combination with a chiral nu...

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Detalles Bibliográficos
Autores principales: Sallio, Romain, Lebrun, Stéphane, Capet, Frédéric, Agbossou-Niedercorn, Francine, Michon, Christophe, Deniau, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852534/
https://www.ncbi.nlm.nih.gov/pubmed/29623121
http://dx.doi.org/10.3762/bjoc.14.46