Triflic Acid Catalyzed Intermolecular α-Amination of Pterolactams to Give 5-Arylaminopyrrolidinones via N-Acyliminium Species - Normandie Université Access content directly
Journal Articles SYNLETT Year : 2016

Triflic Acid Catalyzed Intermolecular α-Amination of Pterolactams to Give 5-Arylaminopyrrolidinones via N-Acyliminium Species

Abstract

A mild and efficient α-aza-amidoalkylation for the synthesis of 5-arylaminopyrrolidinones is presented. The key step of this reaction is the intermolecular interception of an N-acyliminium species, generated under the acidic conditions, with nitrogen nucleophiles such as N-silylamines. © Georg Thieme Verlag Stuttgart New York.
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hal-02413305 , version 1 (16-12-2019)

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Gina-Mirabela Dumitriu, Elena Bîcu, Ulku Eryuruk, Dalila Belei, Benoît Rigo, et al.. Triflic Acid Catalyzed Intermolecular α-Amination of Pterolactams to Give 5-Arylaminopyrrolidinones via N-Acyliminium Species. SYNLETT, 2016, 27 (6), pp.934-940. ⟨10.1055/s-0035-1561333⟩. ⟨hal-02413305⟩
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