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
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.

Identifiants

pubmed: 30534735
doi: 10.1039/c8cc08821g
doi:

Types de publication

Journal Article

Langues

eng

Pagination

338-341

Auteurs

Claire Empel (C)

RWTH Aachen University, Institute of Organic Chemistry, Landoltweg 1, D-52074 Aachen, Germany. rene.koenigs@rwth-aachen.de.

Classifications MeSH