Direct introduction of a naphthalene-1,8-diamino boryl [B(dan)] group by a Pd-catalysed selective boryl transfer reaction

Chem Commun (Camb). 2015 Apr 4;51(26):5656-9. doi: 10.1039/c5cc00231a.

Abstract

A non-symmetrical diboron reagent, B(pin)-B(dan), has been utilised in the Pd-catalysed borylation of aryl bromides and chlorides. Remarkably selective formation of aryl-B(dan) bonds is established. This represents a direct and efficient way to introduce masked boronic acids. The synthetic usefulness of this reaction is demonstrated in the preparation of boron-differentiated di- and polyboron compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Boron Compounds / chemical synthesis*
  • Boron Compounds / chemistry
  • Catalysis
  • Hydrocarbons, Brominated / chemistry*
  • Hydrocarbons, Chlorinated / chemistry*
  • Molecular Structure
  • Palladium / chemistry*

Substances

  • Boron Compounds
  • Hydrocarbons, Brominated
  • Hydrocarbons, Chlorinated
  • Palladium