M. Abdaoui et al., SYNTHESIS OF 2-CHLOROETHYLNITROSOSULFAMIDES (CENS) VIA A TRANSSULFAMOYLATION REACTION, Phosphorus, sulfur and silicon and the related elements, 118, 1996, pp. 39-47
In order to synthesize the series of 2-chloroethylnitrososulfamides (C
ENS), a procedure using the nucleophilic exchange of an activating gro
up of both the sulfamoyl esters and amides by several amines was devel
oped. The N-oxysuccinimide sulfamate ester was revealed as the most re
active sulfamoyl group donor. This transsulfamoylation procedure allow
s the preparation of title compounds, especially the derivatives of am
ino acid esters in two steps in a 75-80% yield.