108429-87-4

Upstream product

• 108429-96-5 methyl N-(2-ethoxypent-4-enyl)acetimidate 
• 108429-80-7 1-ethoxybut-3-enyl cyanide 
• 34837-55-3 Phenylselenyl bromide 
• 10602-36-5 3-butenal 1,1-diethylacetal 
• 108430-00-8 N-acetyl-4-ethoxy-(2-phenylselenomethyl)pyrrolidine 
• 1666-13-3 diphenyl diselenide 

Relevant academic research and scientific papers

Intramolecular Amidoselenation of N-Alkenyl Imidates to N-Heterocycles

The reactions of N-alkenyl imidates with benzeneselenenyl chloride and bromide in chloroform at ambient temperature afford pyrrolidine and piperidine derivatives having a phenylseleno moiety in good to excellent yields under neutral conditions.The key step of this new reaction consists of an intramolecular carbon-nitrogen bond formation and a simultaneous carbon-oxygen bond fission.