951037-87-9

Downstream Products

• 1085965-72-5 tert-butyl (4R,2E)-4-hydroxy-2-isobutyl-5-[N-(2,4,6-trimethylphenylsulfonyl)amino]pent-2-enoate 
• 1085965-70-3 tert-butyl (2R,3S,4S)-3,4-epoxy-2-isobutyl-5-[N-(2,4,6-trimethylphenylsulfonyl)amino]pentanoate 
• 1085965-67-8 tert-butyl (E)-2-isobutyl-5-[N-(2,4,6-trimethylphenylsulfonyl)amino]pent-2-enoate 
• 1085965-66-7 tert-butyl (S)-2-isobutyl-5-[N-(2,4,6-trimethylphenyl)sulfonylamino]pentanoate 
• 1085965-73-6 tert-butyl (4S,2E)-4-hydroxy-2-isobutyl-5-[N-(2,4,6-trimethylphenylsulfonyl)amino]pent-2-enoate 
• 1085965-71-4 tert-butyl (2R,3R,4R)-3,4-epoxy-2-isobutyl-5-[N-(2,4,6-trimethylphenylsulfonyl)amino]pentanoate 
• 659735-97-4 C₂₃H₂₄F₃NSO₆ 
• 659735-88-3 phenylmethyl (2E)-3-((2S)-1-((2,4,6-trimethylphenyl)sulfonyl)-2-aziridinyl)prop-2-enoate 

Relevant academic research and scientific papers

Versatile use of acid-catalyzed ring-opening of β-aziridinyl-α,β-enoates to stereoselective synthesis of peptidomimetics

Treatment of N-arylsulfonylaziridines bearing α,β-unsaturated esters with alcohols, thiols or weak acids such as AcOH in the presence of catalytic amount of Lewis acids affords regio- and stereoselectively ring-opened products, such as δ-aminated γ-alkoxy