Selective Pinacol-Coupling Reaction using ...
Type de document :
Article dans une revue scientifique
DOI :
PMID :
URL permanente :
Titre :
Selective Pinacol-Coupling Reaction using a Continuous Flow System
Auteur(s) :
Sotto, Nicolas [Auteur]
Cazorla, Clement [Auteur]
Villette, Carole [Auteur]
Billamboz, Muriel [Auteur]
Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Len, Christophe [Auteur]
Cazorla, Clement [Auteur]
Villette, Carole [Auteur]
Billamboz, Muriel [Auteur]
Facteurs de Risque et Déterminants Moléculaires des Maladies liées au Vieillissement - U 1167 [RID-AGE]
Len, Christophe [Auteur]
Titre de la revue :
The Journal of organic chemistry
Nom court de la revue :
J. Org. Chem.
Numéro :
81
Pagination :
11065-11071
Date de publication :
2016-11-18
ISSN :
0022-3263
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
The first continuous flow pinacol coupling reaction of carbonyl compounds was successfully achieved within only 2 min during a single pass through a cartridge filled with zinc(0). The optimized method allowed the efficient ...
Lire la suite >The first continuous flow pinacol coupling reaction of carbonyl compounds was successfully achieved within only 2 min during a single pass through a cartridge filled with zinc(0). The optimized method allowed the efficient production of gram-scale value-added compounds with high productivity. The developed methodology is efficient for aromatic or α,β-unsaturated aldehydes but gives moderate results for more stable acetophenone derivatives. Moreover, the flow method displayed better results in terms of yield and selectivity in comparison to the corresponding batch methodology.Lire moins >
Lire la suite >The first continuous flow pinacol coupling reaction of carbonyl compounds was successfully achieved within only 2 min during a single pass through a cartridge filled with zinc(0). The optimized method allowed the efficient production of gram-scale value-added compounds with high productivity. The developed methodology is efficient for aromatic or α,β-unsaturated aldehydes but gives moderate results for more stable acetophenone derivatives. Moreover, the flow method displayed better results in terms of yield and selectivity in comparison to the corresponding batch methodology.Lire moins >
Audience :
Internationale
Vulgarisation :
Non
Équipe(s) de recherche :
Therapeutic innovation targetting inflammation
Date de dépôt :
2019-05-17T13:08:37Z
2021-05-12T11:40:32Z
2021-05-12T11:40:32Z