Gold(i) catalysed regio- and stereoselective ...
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Article dans une revue scientifique: Article original
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Title :
Gold(i) catalysed regio- and stereoselective intermolecular hydroamination of internal alkynes: towards functionalised azoles
Author(s) :
Michon, Christophe [Auteur]
Unité de Catalyse et de Chimie du Solide (UCCS) - UMR 8181
Gilbert, Joachim [Auteur]
Trivelli, Xavier [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle (UGSF) - UMR 8576
Nahra, Fady [Auteur]
Cazin, Catherine S. J. [Auteur]
Agbossou-Niedercorn, Francine [Auteur]
Nolan, Steven P. [Auteur]
Unité de Catalyse et de Chimie du Solide (UCCS) - UMR 8181
Gilbert, Joachim [Auteur]
Trivelli, Xavier [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle (UGSF) - UMR 8576
Nahra, Fady [Auteur]
Cazin, Catherine S. J. [Auteur]
Agbossou-Niedercorn, Francine [Auteur]
Nolan, Steven P. [Auteur]
Journal title :
Organic & Biomolecular Chemistry
Abbreviated title :
Org. Biomol. Chem.
Publication date :
2019-03-27
ISSN :
1477-0539
HAL domain(s) :
Chimie/Chimie de coordination
English abstract : [en]
Gold(i) catalysed regio- and stereoselective intermolecular hydroamination of internal alkynes was developed for the effective synthesis of a series of (Z)-functionalised vinylazoles under solvent free conditions. The ...
Show more >Gold(i) catalysed regio- and stereoselective intermolecular hydroamination of internal alkynes was developed for the effective synthesis of a series of (Z)-functionalised vinylazoles under solvent free conditions. The catalytic hydrogenation of the resulting enamines leads to substituted saturated azoles in good yields.Show less >
Show more >Gold(i) catalysed regio- and stereoselective intermolecular hydroamination of internal alkynes was developed for the effective synthesis of a series of (Z)-functionalised vinylazoles under solvent free conditions. The catalytic hydrogenation of the resulting enamines leads to substituted saturated azoles in good yields.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CNRS
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Centrale Lille
ENSCL
Univ. Artois
Université de Lille
Collections :
Research team(s) :
Méthodologie organométallique pour la catalyse homogène (MOCAH)
Submission date :
2022-03-02T07:13:37Z
2024-01-15T16:14:51Z
2024-01-15T16:14:51Z
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