Login / Signup

Amidoboronates: bringing together the synthesis of BN-heterocycles via a reductive coupling and dynamic covalent chemistry.

Anna J McConnell
Published in: Dalton transactions (Cambridge, England : 2003) (2023)
This Perspective describes how amidoboronates open up new chemical space spanning the areas of BN-heterocycles and dynamic covalent chemistry. BN-containing heterocycles offer the potential to access new properties and reactivity compared to their C-C analogues. Amidoboronates are introduced as a new class of B-N heterocycles that can be synthesised in three isomeric forms ( meso 5 , rac 5 and rac 6 ) from the reductive coupling of N -aryl iminoboronates. Furthermore, initial investigations on the dynamic covalent chemistry of amidoboronates are discussed, such as the reversibility of C-C bond formation following the reductive coupling and tuning the rac 5 / rac 6 ratio via dynamic covalent B-N and B-O bonds.
Keyphrases
  • room temperature
  • cell migration
  • minimally invasive
  • human health