Dealkylative intercepted rearrangement reactions of sulfur ylides.
Journal
Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838
Informations de publication
Date de publication:
02 Jan 2019
02 Jan 2019
Historique:
pubmed:
12
12
2018
medline:
12
12
2018
entrez:
12
12
2018
Statut:
ppublish
Résumé
Sulfur ylides are well-known to undergo sigmatropic rearrangement reaction. Herein, we describe a novel reactivity of sulfur ylides, which provides access to the product of a formal functional group metathesis upon dealkylative interception of the rearrangement process. Using a simple iron catalyst and in situ generated diazoalkanes this method provides access to α-mercaptoacetonitrile derivatives.
Types de publication
Journal Article
Langues
eng