Abstract
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.
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CITATION STYLE
Khumalo, M. F., Akpan, E. D., Chinthakindi, P. K., Brasil, E. M., Rajbongshi, K. K., Makatini, M. M., … Arvidsson, P. I. (2018). Synthesis of novel 1,2,4-thiadiazinane 1,1-dioxides via three component SuFEx type reaction. RSC Advances, 8(65), 37503–37507. https://doi.org/10.1039/C8RA07627H
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