852332-91-3Relevant academic research and scientific papers
Optically pure trans-2,3-disubstituted N-sulfinyl aziridines. Regio- and stereoselective opening mediated by the sulfinyl group
Arroyo, Yolanda,Meana, ángela,Rodríguez, J. Félix,Santos, Mercedes,Sanz-Tejedor, M. Ascensión,García-Ruano, José L.
, p. 8525 - 8532 (2007/10/03)
A new entry to optically pure trans-2,3-disubstituted N-sulfinyl aziridines starting from 1,2-aminosulfides, involving formation of a sulfonium salt intermediate followed by intramolecular nucleophilic attack by the sulfinamide nitrogen atom, is reported.
Synthesis of optically pure 1,2-diaryl- and 1,2-alkylaryl-1,2-amino sulfides
Arroyo, Yolanda,Meana, Angela,Rodriguez, J. Felix,Santos, Mercedes,Sanz-Tejedor, M. Ascension,Garcia Ruano, Jose L.
, p. 3914 - 3920 (2007/10/03)
The reactions of the lithium (S)-α-(methylthio)-2-(p-toluenesulfinyl) benzyl carbanion with (S)-N-p-tolylsulfinyl aldimines evolve in a completely stereoselective manner providing a one-step synthesis of enantiomerically pure anti-1,2-disubstituted 1,2-am
