Regio- and diastereoselective Pd-catalyzed synthesis of C2-aryl glycosides.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
30 Jun 2020
Historique:
pubmed: 29 5 2020
medline: 29 5 2020
entrez: 29 5 2020
Statut: ppublish

Résumé

An efficient regio- and diastereoselective arylation method of readily available 2,3-glycals with various aryl iodides has been established. Using the Pd(OAc)2/AsPh3 precatalytic system, this protocol proved to be general to prepare a variety of substituted C2-aryl glycosides in good yields with complete diastereoselectivity.

Identifiants

pubmed: 32463030
doi: 10.1039/d0cc02175j
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7175-7178

Auteurs

Juba Ghouilem (J)

Universite Paris-Saclay, CNRS, BioCIS, 92290, Châtenay-Malabry, France. samir.messaoudi@universite-paris-saclay.fr.

Rémi Franco (R)

Universite Paris-Saclay, CNRS, BioCIS, 92290, Châtenay-Malabry, France. samir.messaoudi@universite-paris-saclay.fr.

Pascal Retailleau (P)

Institut de Chimie des Substances Naturelles, CNRS UPR 2301, Universite Paris-Saclay, avenue de la terrasse, 91198 Gif-sur-Yvette, France.

Mouad Alami (M)

Universite Paris-Saclay, CNRS, BioCIS, 92290, Châtenay-Malabry, France. samir.messaoudi@universite-paris-saclay.fr.

Vincent Gandon (V)

Université Paris-Saclay, CNRS, ICMMO, 91405, Orsay Cedex, France. vincent.gandon@universite-paris-saclay.fr and Laboratoire de Chimie Moléculaire (LCM), CNRS UMR 9168, Ecole Polytechnique, Institut Polytechnique de Paris, route de Saclay, 91128 Palaiseau Cedex, France.

Samir Messaoudi (S)

Universite Paris-Saclay, CNRS, BioCIS, 92290, Châtenay-Malabry, France. samir.messaoudi@universite-paris-saclay.fr.

Classifications MeSH