948915-91-1

Upstream product

• 948915-96-6 C₂₉H₄₉N₄O₇ 
• 583827-05-8 C₁₉H₂₇N₂O₃ 
• 488703-60-2 (1S,2S)-2-((tert-butoxycarbonyl)amino)cyclohexane-1-carboxylic acid 
• 948915-90-0 C₃₀H₅₁N₄O₇ 
• 948915-95-5 C₂₂H₃₈N₃O₆ 
• 948915-87-5 C₂₃H₄₀N₃O₆ 
• 583827-08-1 (3S,4S)-4-[(1'S)-phenylethyl]amino-3-methoxycarbonyl-2,2,6,6-tetramethyl-piperidine-1-oxyl hydrochloride 
• 583827-08-1 (3R,4S)-4-[(1'S)-phenylethyl]amino-3-methoxycarbonyl-2,2,6,6-tetramethyl-piperidine-1-oxyl hydrochloride 
• 864150-31-2 (3R,4S)-4-amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic acid methyl ester 
• 77874-89-6 2,2,6,6-tetramethyl-3-methoxycarbonyl-4-piperidone-1-oxyl 

Downstream Products

• 948915-97-7 C₃₆H₆₀N₅O₈ 

Relevant academic research and scientific papers

Synthesis of enantiomerically pure cis- and trans-4-amino-1-oxyl-2,2,6,6- tetramethylpiperidine-3-carboxylic acid: A spin-labelled, cyclic, chiral β-amino acid, and 3D-structural analysis of a doubly spin-labelled β-hexapeptide

Animation of 3-carboxymethyl-1-oxyl-2,2,6,6-tetramethyl-4-piperidone (1) with either (R)- or (S)-α-methylbenzylamine gave corresponding enamines 2. Whereas the reduction with NaBH3CN/CH3COOH afforded predominantly a mixture of two po