948915-89-7

Upstream product

• 583827-05-8 C₁₉H₂₇N₂O₃ 
• 488703-60-2 (1S,2S)-2-((tert-butoxycarbonyl)amino)cyclohexane-1-carboxylic acid 
• 77874-89-6 2,2,6,6-tetramethyl-3-methoxycarbonyl-4-piperidone-1-oxyl 
• 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 
• 864150-33-4 (3R,4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2,2,6,6-tetramethylpiperidine-1-oxyl-3-carboxylic acid 
• 864150-31-2 (3R,4S)-4-amino-1-oxyl-2,2,6,6-tetramethylpiperidine-3-carboxylic acid methyl ester 
• 948915-88-6 C₃₃H₄₂N₃O₆ 

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