Visible-light-driven carboxylic amine ...
Document type :
Article dans une revue scientifique: Article original
PMID :
Permalink :
Title :
Visible-light-driven carboxylic amine protocol (clap) for the synthesis of 2-substituted piperazines under batch and flow conditions
Author(s) :
Gueret, Robin [Auteur]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Pelinski, Lydie [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Bousquet, Till [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Sauthier, Mathieu [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Ferey, Vincent [Auteur]
SANOFI Recherche
Bigot, Antony [Auteur]
Sanofi [Vitry-sur-Seine]
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Pelinski, Lydie [Auteur]

Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Bousquet, Till [Auteur]

Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Sauthier, Mathieu [Auteur]

Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Ferey, Vincent [Auteur]
SANOFI Recherche
Bigot, Antony [Auteur]
Sanofi [Vitry-sur-Seine]
Journal title :
Organic Letters
Abbreviated title :
Org. Lett.
Volume number :
22
Pages :
5157–5162
Publisher :
American Chemical Society (ACS)
Publication date :
2020-06-23
ISSN :
1523-7052
English keyword(s) :
Aldehydes
Amines
Chemical reactions
Irradiation
Photocatalysts
Amines
Chemical reactions
Irradiation
Photocatalysts
HAL domain(s) :
Chimie/Catalyse
English abstract : [en]
Piperazines are privileged scaffolds in medicinal chemistry. Disclosed herein is a visible-light-promoted decarboxylative annulation protocol between a glycine-based diamine and various aldehydes to access 2-aryl, 2-heteroaryl, ...
Show more >Piperazines are privileged scaffolds in medicinal chemistry. Disclosed herein is a visible-light-promoted decarboxylative annulation protocol between a glycine-based diamine and various aldehydes to access 2-aryl, 2-heteroaryl, as well as 2-alkyl piperazines. The iridium-based complex [Ir(ppy)2(dtbpy)]PF6 and carbazolyl dicyanobenzene 4CzIPN were found to be the photocatalysts of choice to efficiently perform the transformation under mild conditions, whether in batch or in continuous mode.Show less >
Show more >Piperazines are privileged scaffolds in medicinal chemistry. Disclosed herein is a visible-light-promoted decarboxylative annulation protocol between a glycine-based diamine and various aldehydes to access 2-aryl, 2-heteroaryl, as well as 2-alkyl piperazines. The iridium-based complex [Ir(ppy)2(dtbpy)]PF6 and carbazolyl dicyanobenzene 4CzIPN were found to be the photocatalysts of choice to efficiently perform the transformation under mild conditions, whether in batch or in continuous mode.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Other project(s) or funding source(s) :
Sanofi
CNRS
Chevreul Institute (FR 2638)
Ministère de l’Enseignement Supérieur et de la Recherche
Région Nord Pas-de-Calais
FEDER
CNRS
Chevreul Institute (FR 2638)
Ministère de l’Enseignement Supérieur et de la Recherche
Région Nord Pas-de-Calais
FEDER
Administrative institution(s) :
CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Collections :
Research team(s) :
Catalyse et synthèse éco-compatible (CASECO)
Submission date :
2022-03-02T07:13:36Z
2023-11-28T15:47:25Z
2023-11-28T15:47:25Z
Files
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