A new asymmetric synthesis of 2,6-cis-diarylated ...
Document type :
Article dans une revue scientifique: Article original
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Title :
A new asymmetric synthesis of 2,6-cis-diarylated piperidines
Author(s) :
Sallio, Romain [Auteur]
Lebrun, Stephane [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Deniau, Eric [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Sallio, Romain [Auteur]
Lebrun, Stephane [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Deniau, Eric [Auteur]
Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181
Unité de Catalyse et Chimie du Solide - UMR 8181 [UCCS]
Sallio, Romain [Auteur]
Journal title :
Tetrahedron: Asymmetry
Abbreviated title :
Tetrahedron. Asymmetry
Volume number :
26
Pages :
209-213
Publication date :
2015
ISSN :
0957-4166
HAL domain(s) :
Chimie/Catalyse
English abstract : [en]
A new synthetic approach to a variety of enantioenriched 2,6-cis-diarylated piperidines has been developed. This new methodology hinges upon the diastereoselective reduction of enantioenriched endocyclic enecarbamates ...
Show more >A new synthetic approach to a variety of enantioenriched 2,6-cis-diarylated piperidines has been developed. This new methodology hinges upon the diastereoselective reduction of enantioenriched endocyclic enecarbamates obtained through a two step sequence involving a Suzuki–Miyaura cross coupling reaction between an aminovinyl phosphate and a variety of (hetero)aromatic boronic acids.Show less >
Show more >A new synthetic approach to a variety of enantioenriched 2,6-cis-diarylated piperidines has been developed. This new methodology hinges upon the diastereoselective reduction of enantioenriched endocyclic enecarbamates obtained through a two step sequence involving a Suzuki–Miyaura cross coupling reaction between an aminovinyl phosphate and a variety of (hetero)aromatic boronic acids.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
ENSCL
CNRS
Centrale Lille
Univ. Artois
Université de Lille
CNRS
Centrale Lille
Univ. Artois
Université de Lille
Collections :
Research team(s) :
Catalyse et synthèse éco-compatible (CASECO)
Submission date :
2019-09-25T14:04:43Z
2023-11-21T10:10:33Z
2023-11-23T12:22:33Z
2023-12-05T18:40:09Z
2023-11-21T10:10:33Z
2023-11-23T12:22:33Z
2023-12-05T18:40:09Z
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