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Oxetane Synthesis via Alcohol C–H Functionalization

[Image: see text] Oxetanes are strained heterocycles with unique properties that have triggered significant advances in medicinal chemistry. However, their synthesis still presents significant challenges that limit the use of this class of compounds in practical applications. In this Letter, we pres...

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Detalles Bibliográficos
Autores principales: Paul, Subhasis, Filippini, Dario, Ficarra, Filippo, Melnychenko, Heorhii, Janot, Christopher, Silvi, Mattia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375527/
https://www.ncbi.nlm.nih.gov/pubmed/37462721
http://dx.doi.org/10.1021/jacs.3c04891
Descripción
Sumario:[Image: see text] Oxetanes are strained heterocycles with unique properties that have triggered significant advances in medicinal chemistry. However, their synthesis still presents significant challenges that limit the use of this class of compounds in practical applications. In this Letter, we present a methodology that introduces a new synthetic disconnection to access oxetanes from native alcohol substrates. The generality of the approach is demonstrated by the application in late-stage functionalization chemistry, which is further exploited to develop a single-step synthesis of a known bioactive synthetic steroid derivative that previously required at least four synthetic steps from available precursors.