Highly chemoselective homologative assembly of the α-substituted methylsulfinamide motif from

Journal

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

Informations de publication

Date de publication:
14 Sep 2023
Historique:
medline: 30 8 2023
pubmed: 30 8 2023
entrez: 30 8 2023
Statut: epublish

Résumé

α-Substituted methylsulfinamide are prepared through the homologation of electrophilic

Identifiants

DOI: 10.1039/d3cc03326k PMID: 37644820
pubmed: 37644820
doi: 10.1039/d3cc03326k
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

11065-11068

Auteurs

Monika Malik (M)

Department of Pharmaceutical Sciences, Division of Pharmaceutical Chemistry, University of Vienna, Josef-Holaubek-Platz 2, 1090, Vienna, Austria. vittorio.pace@univie.ac.at.

Raffaele Senatore (R)

Department of Pharmaceutical Sciences, Division of Pharmaceutical Chemistry, University of Vienna, Josef-Holaubek-Platz 2, 1090, Vienna, Austria. vittorio.pace@univie.ac.at.

Davide Castiglione (D)

Department of Chemistry, Via Giuria 7, University of Turin, Turin 10125, Italy.

Alexander Roller-Prado (A)

Department of Inorganic Chemistry - Functional Materials, University of Vienna, Waehringerstrasse 42, 1090, Vienna, Austria.

Vittorio Pace (V)

Department of Pharmaceutical Sciences, Division of Pharmaceutical Chemistry, University of Vienna, Josef-Holaubek-Platz 2, 1090, Vienna, Austria. vittorio.pace@univie.ac.at.
Department of Chemistry, Via Giuria 7, University of Turin, Turin 10125, Italy.
ORCID: 0000-0003-3037-5930

Classifications MeSH