198547-54-5

Upstream product

• 1666-13-3 diphenyl diselenide 
• 198547-63-6 N-allyl-N-benzyl-2-bromo-2,2-difluoroacetamide 
• 100-46-9 benzylamine 

Relevant academic research and scientific papers

Visible-Light-Induced, Catalyst-Free Radical Cross-Coupling Cyclization of N-Allylbromodifluoroacetamides with Disulfides or Diselenides

A visible-light-induced, catalyst-free radical cross-coupling cyclization of diselenides or disulfides with N-allylbromodifluoroacetamide has been developed. This developed protocol exhibits good functional group tolerance and affords a variety of 4-thio-

Generation and intramolecular cyclization of difluoroalkyl radicals via single electron transfer from the benzeneselenolate anion: Synthesis of α,α-difluoro-γ-lactams

Several α,α-difluoro-γ-lactams (2) were prepared by radical cyclization of amides (1) which were initiated by a single transfer(SET) process from the benzenesclenolate anion. Deselenation of these lactams (2) gave the corresponding α,α-difluoro-β-exomethylene lactams (8).