Hydroboration of isocyanides with diisopropylaminoborane: general access to ambiphilic boron-based glycine isosteres

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Abstract
We report a straightforward and catalyst-free synthetic methodology for accessing α-aminoboron compounds incorporating the N–CH 2 –B motif through the double hydroboration of various isocyanides using diisopropylaminoborane (DIAB).
Funding Information
  • Centre National de la Recherche Scientifique
  • Agence Nationale de la Recherche (p18018)
  • Agence Nationale de la Recherche (p20038)
  • Institut de chimie (SILVA)

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