Ni/Photoredox-Dual-Catalyzed Functionalization of 1-Thiosugars.


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
05 07 2019
Historique:
pubmed: 30 6 2019
medline: 30 6 2019
entrez: 29 6 2019
Statut: ppublish

Résumé

A general protocol for functionalization of glycosyl thiols has been reported. This protocol is based on a single-electron Ni/photoredox dual-catalyzed cross coupling between 1-thiosugars and a broad range of aryl bromides and iodides as well as alkenyl and alkynyl halides. This base-free method gives access to a series of functionalized thioglycosides in moderate to excellent yields with a perfect control of the anomeric configuration. Moreover, it has been shown that this methodology may be transposed successfully to the continuous-flow photoredox chemistry.

Identifiants

pubmed: 31247796
doi: 10.1021/acs.orglett.9b01730
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5132-5137

Auteurs

Mingxiang Zhu (M)

BioCIS , Université Paris-Sud, CNRS, University Paris-Saclay , Châtenay-Malabry , France.

Guillaume Dagousset (G)

Institut Lavoisier de Versailles, UMR 8180 , Université de Versailles Saint-Quentin , 78035 Cedex Versailles , France.

Mouad Alami (M)

BioCIS , Université Paris-Sud, CNRS, University Paris-Saclay , Châtenay-Malabry , France.

Emmanuel Magnier (E)

Institut Lavoisier de Versailles, UMR 8180 , Université de Versailles Saint-Quentin , 78035 Cedex Versailles , France.

Samir Messaoudi (S)

BioCIS , Université Paris-Sud, CNRS, University Paris-Saclay , Châtenay-Malabry , France.

Classifications MeSH