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Straightforward Access to Thiocyanates via Dealkylative Cyanation of Sulfoxides

[Image: see text] Thiocyanates, versatile building blocks in organic synthesis, are shown to be easily accessible via an interrupted Pummerer reaction of sulfoxides. This facile dealkylative functionalization proceeds under mild conditions through electrophilic activation of the sulfoxide partner. T...

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Detalles Bibliográficos
Autores principales: Todorović, Uroš, Klose, Immo, Maulide, Nuno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022320/
https://www.ncbi.nlm.nih.gov/pubmed/33724046
http://dx.doi.org/10.1021/acs.orglett.1c00460
Descripción
Sumario:[Image: see text] Thiocyanates, versatile building blocks in organic synthesis, are shown to be easily accessible via an interrupted Pummerer reaction of sulfoxides. This facile dealkylative functionalization proceeds under mild conditions through electrophilic activation of the sulfoxide partner. The resulting thiocyanate itself can serve as a handle for diversification in a straightforward one-pot procedure.