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Metal-Free C-H Borylation of N-Heteroarenes by Boron Trifluoride.

Vladimir IashinDénes BertaKonstantin ChernichenkoMartin NiegerKarina MoslovaImre PápaiTimo Repo
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2020)
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 BF3 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.
Keyphrases
  • transition metal
  • electron transfer
  • crystal structure
  • room temperature
  • case control