87581-19-9

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 99-33-2 3,5-dinitrobenoyl chloride 
• 99-34-3 3,5-dinitrobenzoic acid 

Downstream Products

• 63378-99-4 (3,5-dinitrophenyl)(2-methylaziridin-1-yl)methanone 
• 1407164-65-1 (S)-(3,5-dinitrophenyl)(2-isobutylaziridin-1-yl)methanone 
• 1335200-11-7 (S)-(3,5-dinitrophenyl)(2-isopropylaziridin-1-yl)methanone 
• 1407164-57-1 (2-(3-((tert-butyldiphenylsilyl)oxy)propyl)aziridin-1-yl)(3,5-dinitrophenyl)methanone 
• 1407164-53-7 (2-cyclohexylaziridin-1-yl) (3,5-dinitrophenyl)methanone 
• 1407164-50-4 (3,5-dinitrophenyl)(2-isobutylaziridin-1-yl)methanone 
• 1407164-51-5 (R)-(3,5-dinitrophenyl)(2-isobutylaziridin-1-yl)methanone 
• 1335199-91-1 (3,5-dinitrophenyl)(2-hexylaziridin-1-yl)methanone 
• 1407164-48-0 (S)-N-(2-chlorooctyl)-3,5-dinitrobenzamide 
• 1407164-69-5 (S)-3,5-dinitro-N-(2-(phenylamino)octyl)benzamide 
• 1407164-47-9 (R)-(3,5-dinitrophenyl)(2-hexylaziridin-1-yl)methanone 
• 1407164-67-3 (R)-2-(3,5-dinitrophenyl)-5-hexyl-4,5-dihydrooxazole 

Relevant academic research and scientific papers

Chiral Recognition of Peptide Enantiomers by Cinchona Alkaloid Derived Chiral Selectors: Mechanistic Investigations by Liquid Chromatography, NMR Spectroscopy, and Molecular Modeling

The chiral recognition mechanism of a cinchona alkaloid based chiral selector for N-protected peptide enantiomers was investigated. A chiral stationary phase derived from this selector was employed for liquid chromatographic enantiomer separations. It sho

Scalable synthesis of N -acylaziridines from N -tosylaziridines

N-Acylaziridines are important starting materials for the synthesis of chiral amine derivatives. The traditional methods for producing these activated aziridines have significant drawbacks. The gram scale synthesis of N-acylaziridines by deprotection of N