850668-97-2

Upstream product

• 116547-92-3 N-(2-iodophenyl)methanesulfonamide 
• 850668-96-1 N-[(Z)-4-(tert-butyldiphenylsilanyloxy)but-2-enyl]-N-(2-iodophenyl)methanesulfonamide 

Downstream Products

• 850668-92-7 N-(2-iodophenyl)-N-[(Z)-4-methoxy-but-2-enyl]methanesulfonamide 
• 850668-98-3 N-[(Z)-4-chloro-but-2-enyl]-N-(2-iodophenyl)methanesulfonamide 

Relevant academic research and scientific papers

Highly efficient reduction of unactivated aryl and alkyl iodides by a ground-state neutral organic electron donor

Electron-transfer reductions of unactivated aryl and alkyl iodides with a neutral ground-state organic molecule are reported. The reducing agent 1 is formed in two steps from N-methylbenzimidazole using very simple chemistry, and subsequent treatment of the iodoalkane or-arene with 1 affords cyclized products (see scheme).