Cargando…

Metal‐Free C−H Borylation of N‐Heteroarenes by Boron Trifluoride

Organoboron compounds are essential reagents in modern C−C coupling reactions. Their synthesis via catalytic C−H borylation by main group elements is emerging as a powerful tool alternative to transition metal based catalysis. Herein, a straightforward metal‐free synthesis of aryldifluoroboranes fro...

Descripción completa

Detalles Bibliográficos
Autores principales: Iashin, Vladimir, Berta, Dénes, Chernichenko, Konstantin, Nieger, Martin, Moslova, Karina, Pápai, Imre, Repo, Timo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702085/
https://www.ncbi.nlm.nih.gov/pubmed/32478432
http://dx.doi.org/10.1002/chem.202001436
Descripción
Sumario:Organoboron compounds are essential reagents in modern C−C coupling reactions. Their synthesis via catalytic C−H borylation by main group elements is emerging as a powerful tool alternative to transition metal based catalysis. Herein, a straightforward metal‐free synthesis of aryldifluoroboranes from BF(3) and heteroarenes is reported. The reaction is assisted by sterically hindered amines and catalytic amounts of thioureas. According to computational studies the reaction proceeds via frustrated Lewis pair (FLP) mechanism. The obtained aryldifluoroboranes are further stabilized against destructive protodeborylation by converting them to the corresponding air stable tetramethylammonium organotrifluoroborates.