61415-35-8

Upstream product

• 35462-98-7 <α-13C>phenethyl alcohol 

Downstream Products

• 67519-32-8 2-<1-(13C)-Phenethyl>-1.3-<13C>-malonsaeure-diethylester 
• 61415-37-0 <1-13C>-2-Phenylaethen 
• 213481-40-4 [2,3,7,8,12,13,17,18-octachloro-5,10,15,20-tetrakis(p-tert-butylphenyl)porphyrinato]phenethyl-1-⁽¹³⁾C-rhodium(III) 
• 549548-77-8 (E)-(β-13C)-β-bromostyrene 

Relevant academic research and scientific papers

Reactions of nitroxides with metalloporphyrin alkyls bearing beta hydrogens: Aliphatic carbon-carbon bond activation by metal centered radicals

Nitroxide-induced beta-hydrogen atom abstraction and beta-elimination of rhodium porphyrin alkyls have been observed. Rhodium(II) porphyrin radical were proposed intermediates to form first and subsequently reacted via aliphatic carbon-carbon bond activation with alkyl substituted nitroxides to yield rhodium porphyrin alkyl complexes.