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Diborylmethyl Group as a Transformable Building Block for the Diversification of Nitrogen-Containing Molecules.

Chiwon HwangYeosan LeeMinjae KimYounggyu SeoSeung Hwan Cho
Published in: Angewandte Chemie (International ed. in English) (2022)
The development of new approaches to installing diverse carbon fragments to a nitrogen atom has attracted considerable attention in chemical science. While numerous strategies have been devised to forge C(sp 3 )-N bonds, one conceptually powerful and straightforward approach is to insert a transformable sp 3 -carbon unit onto a nitrogen atom for modular diversification. Here we describe the successful synthesis of halo-diborylmethanes and their applications to the preparation of nitrogen-substituted diborylmethanes through their homologative coupling with a variety of nitrogen nucleophiles including biologically relevant molecules. This process exhibits a remarkably broad substrate scope, and the usefulness of the obtained compounds is demonstrated by the modular diversification of the diborylmethyl group to access various nitrogen-containing molecules.
Keyphrases
  • public health
  • molecular dynamics
  • working memory
  • high resolution
  • molecular docking
  • mass spectrometry
  • molecular dynamics simulations
  • liquid chromatography
  • solid phase extraction