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Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C–O Bond Activation

[Image: see text] A magnesium-catalyzed regiodivergent C–O bond cleavage protocol is presented. Readily available magnesium catalysts achieve the selective hydroboration of a wide range of epoxides and oxetanes yielding secondary and tertiary alcohols in excellent yields and regioselectivities. Expe...

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Detalles Bibliográficos
Autores principales: Magre, Marc, Paffenholz, Eva, Maity, Bholanath, Cavallo, Luigi, Rueping, Magnus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458426/
https://www.ncbi.nlm.nih.gov/pubmed/32658463
http://dx.doi.org/10.1021/jacs.0c05917
Descripción
Sumario:[Image: see text] A magnesium-catalyzed regiodivergent C–O bond cleavage protocol is presented. Readily available magnesium catalysts achieve the selective hydroboration of a wide range of epoxides and oxetanes yielding secondary and tertiary alcohols in excellent yields and regioselectivities. Experimental mechanistic investigations and DFT calculations provide insight into the unexpected regiodivergence and explain the different mechanisms of the C–O bond activation and product formation.