3376-29-2

Upstream product

• 3376-42-9 N-benzhydryl-N-benzyl-hydroxylamine 
• 29127-86-4 benzophenone oxime ; sodium salt 
• 620-05-3 iodomethylbenzene 
• 100-46-9 benzylamine 
• 7699-79-8 benzhydrylidene-benzyl-amine 
• 100-39-0 benzyl bromide 
• 574-66-3 Benzophenone oxime 

Downstream Products

• 119-61-9 benzophenone 
• 622-30-0 N-benzyl hydroxylalmine 
• 3376-42-9 N-benzhydryl-N-benzyl-hydroxylamine 

Relevant academic research and scientific papers

Synthesis of 4-Isoxazolines via Visible-Light Photoredox-Catalyzed [3 + 2] Cycloaddition of Oxaziridines with Alkynes

A method for [3 + 2] cycloaddition of oxaziridines with alkynes to form 4-isoxazolines via visible-light photoredox catalysis is described. This method is a greener, atom-economical reaction that tolerates various functional groups and provides good to excellent yield. Moreover, the cyclization products can be conveniently converted into tetrasubstituted allylic alcohols and enamines. A mechanistic study suggests that the reaction involves photoredox-catalyzed in situ generation of a nitrone from the oxaziridine by SET.