99896-08-9

Upstream product

• 158478-40-1 (E)-N-allyl-5-phenylpent-4-en-1-amine 
• 37464-87-2 (5-bromopent-1-enyl)benzene 
• 13159-16-5 5-phenyl-4-penten-1-ol 
• 144220-38-2 trans-N-allyl-N-(benzenesulfenyl)-5-phenylpent-4-enylamine 

Relevant academic research and scientific papers

Synthesis of pyrrolizidines using aminyl radicals generated from sulfenamide precursors

Tandem radical cyclisations of aminyl radicals generated from sulfenamide precursors have been used for the synthesis of pyrrolizidines and other polycyclic nitrogen heterocycles. The aminyl radicals are generated by reaction between sulfenamide precursor

Cyclisation of aminyl radicals using sulfenamide precursors

Sulfenamides react readily with tributyltin hydride to yield aminyl radicals, which undergo intramolecular addition to activated double bonds.