370591-24-5

Upstream product

• 186581-53-3 diazomethane 
• 135822-89-8 N-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-4-methyl-benzenesulfonamide 
• 2635-13-4 1,2-(methylenedioxy)-4-bromobenzene 

Relevant academic research and scientific papers

Ni-Catalyzed Carboxylation of Aziridines en Route to β-Amino Acids

A Ni-catalyzed reductive carboxylation of N-substituted aziridines with CO2 at atmospheric pressure is disclosed. The protocol is characterized by its mild conditions, experimental ease, and exquisite chemo- and regioselectivity pattern, thus unlocking a new catalytic blueprint to access β-amino acids, important building blocks with considerable potential as peptidomimetics.

Catalyst-free aziridination and unexpected homologation of aziridines from imines

Aziridination and unpredicted homologation reaction of N-sulfonylimines were achieved easily with a very simple, rapid and mild procedure through the use of diazomethane without the presence of any catalyst. The method represents an attractive alternative