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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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Detalhes bibliográficos
Publicado no:Beilstein J Org Chem
Main Authors: Sallio, Romain, Lebrun, Stéphane, Capet, Frédéric, Agbossou-Niedercorn, Francine, Michon, Christophe, Deniau, Eric
Formato: Artigo
Idioma:Inglês
Publicado em: Beilstein-Institut 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5852534/
https://ncbi.nlm.nih.gov/pubmed/29623121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.14.46
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