341968-36-3

Upstream product

• 106-95-6 allyl bromide 
• 161776-41-6 1-hydroxy-2-phenyl-2-(2',2',6',6'-tetramethyl-1'-piperidinyloxy)ethane 
• 2564-83-2 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical 
• 507481-64-3 allyl(2-bromo-2-phenylethyl) ether 
• 81913-53-3 1-(2-benzoyloxy-1-phenylethoxy)-2,2,6,6-tetramethylpiperidine 

Relevant academic research and scientific papers

Synthesis and multidimensional NMR characterization of PDMS-b-PS prepared by combined anionic ring-opening and nitroxide-mediated radical polymerization

The synthesis of PDMS-b-PS copolymers by anionic and nitroxide-mediated radical polymerization (NMRP) is discussed. Hydride end-capped PDMS is hydrosilylated with an allylic alkoxyamine to form a TEMPO functional macroinitiator. The macroinitiator is reac

CO-trapping reaction under thermolysis of alkoxyamines: Application to the synthesis of 3,4-cyclopenta-1-tetralones

(Chemical Equation Presented) An efficient one-pot sequence comprising a PRE-mediated radical 5-exo-cyclization, a radical carbonylation, a nitroxide trapping reaction, and a subsequent acid-catalyzed Friedel-Craft-type acylation provides a new entry into