464189-17-1

Upstream product

• 464189-16-0 3-((1,3-dioxoisoindolin-2-yl)oxy)-2,2-dimethylpropanoic acid 
• 108-91-8 cyclohexylamine 
• 17701-61-0 benzyl 2,2-dimethyl-3-hydroxypropanoic acid 
• 14002-80-3 Methyl 2,2-dimethyl-3-hydroxypropionate 
• 4835-90-9 3-Hydroxy-2,2-dimethylpropanoic acid 
• 524-38-9 N-hydroxyphthalimide 
• 464189-15-9 benzyl 3-((1,3-dioxoisoindolin-2-yl)oxy)-2,2-dimethylpropanoate 

Downstream Products

• 464189-13-7 N-(2-cyclohexylcarbamoyl-2-methyl-propoxy)-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-2,2-dimethyl-propionamide 

Relevant academic research and scientific papers

β2,2-aminoxy acids: A new building block for turns and helices

The conformational properties of peptides 1-4 built from 3-aminoxy-2,2-dimethyl-propionic acid, a β2,2-aminoxy acid, were investigated by NMR spectroscopy and X-ray crystallography. A novel β N-O turn involving a nine-membered-ring intramolecular hydrogen bond between NHi+2 and COi was formed in diamides 1 and 2, which was further stabilized by another six-membered-ring intramolecular hydrogen bond between NHi+2 and NOi+1. Triamides 3 and 4 displayed a well-defined helical structure featuring two consecutive β N-O turns. The X-ray structure of 4 revealed that the amide carbonyl group at position i+2 was twisted +65.9° from that at i position, suggesting a novel 1.79 helix. Therefore, β2,2-aminoxy acid can be used as a new building block for turns and helices. Copyright