659735-97-4Relevant academic research and scientific papers
Versatile use of acid-catalyzed ring-opening of β-aziridinyl-α,β-enoates to stereoselective synthesis of peptidomimetics
Tamamura, Hirokazu,Tanaka, Tomohiro,Tsutsumi, Hiroshi,Nemoto, Koji,Mizokami, Satoko,Ohashi, Nami,Oishi, Shinya,Fujii, Nobutaka
, p. 9243 - 9254 (2008/02/09)
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
