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Synthesis of novel 1,2,4-thiadiazinane 1,1-dioxides via three component SuFEx type reaction.

Mzilikazi F KhumaloEkemini D AkpanPraveen K ChinthakindiEdikarlos M BrasilKamal K RajbongshiMaya M MakatiniThavendran GovenderHendrik Gerhardus KrugerTricia NaickerPer I Arvidsson
Published in: RSC advances (2018)
Herein, we report the preparation of 1,2,4-thiadiazinane 1,1-dioxides from reaction of β-aminoethane sulfonamides with dichloromethane, dibromomethane and formaldehyde as methylene donors. The β-aminoethane sulfonamides were obtained through sequential Michael addition of amines to α,β-unsaturated ethenesulfonyl fluorides followed by further DBU mediated sulfur(vi) fluoride exchange (SuFEx) reaction with amines at the S-F bond.
Keyphrases
  • electron transfer
  • drinking water
  • solid phase extraction
  • room temperature
  • mass spectrometry