As azide compounds play a central role in the synthesis of 1,2,3-triazoles in click chemistry, this method is expected to contribute to the efficient development of pharmaceuticals and other ...

Although these "trivalent" platforms enable the efficient synthesis of complex compounds, the selective formation of triazoles using platforms with azide and alkyne moieties remains an unsolved ...

Click chemistry has become an essential tool in applied chemistry due to its simplicity, efficiency, and versatility. This approach to chemical synthesis allows for quick and reliable joining of ...

A controlled/“living” click polymerization method developed by researchers at Institute of Science Tokyo and Nagoya University enables precise chain-growth of AB-type monomers—traditionally limited to ...

The chemists start with an aromatic azide and use a photochemical reaction with ethylaminoethanol, followed by oxidation with N -bromocaprolactam. Only the carbon that was attached to the azide is ...

They made the compounds by reacting sodium azide with pyridines bearing two halogen atoms. This produced nine different fluoro-, chloro-, and bromo-azidopyridines in yields of 24–82%.

Click chemistry has become an essential tool in applied chemistry due to its simplicity, efficiency, and versatility. This approach to chemical synthesis allows for quick and reliable joining of ...