Metal-free catalytic vicinal diamination of alkenes

The development of an intramolecular vicinal diamination protocol using metal-free conditions is discussed. The reaction uses a bromide source to generate a Br(I) catalyst in situ from a benign terminal oxidant such as sodium chlorite. The reaction is of great scope and surpasses the transition-metal catalyses developed so far for these types of reactions.

Random publication image

K. Muñiz

Pure & Appl. Chem. 2013, 85, 755-761
DOI: Go to the journal

Associated ICIQ research group/s:

  • RESEARCH GROUP/S
    Prof. Dr. Kilian Muñiz
Go to the journal
  • SHARE

Let's create a brighter future

Join our team to work with renowned researchers, tackle groundbreaking
projects and contribute to meaningful scientific advancements

Join us!
Board of Trustees:
Member of:
Accredited with:
With the support of: