sulfenyl chloride

sulfenyl chloride

[‚səl′fen·əl ′klȯr‚īd]
(organic chemistry)
Any of a group of well-known organosulfur compounds with the general formula RSCl; although highly reactive compounds, they can generally be synthesized and isolated; examples are trichloromethanesulfenyl chloride and 2,4-dinitrobenzenesulfenyl chloride.
References in periodicals archive ?
Sulfenamides (3-7) were obtained by the reaction of aminoacids hydrochloride in the presence of Et3N with sulfenyl chloride 1 (Scheme.
The reaction mixture was cooled to 0 oC before addition of sulfenyl chloride (1.
Several methods have been reported for the synthesis of sulfenamides including the reaction of sulfenyl chlorides with amines and the reaction of haloamides with thiols [11].
Here, we have reported the synthesis of novel sulfenamides by using the reaction of sulfenyl chlorides with (alpha)-amino esters.
The literature procedure [11] was used for the synthesis of sulfenyl chlorides (Scheme.
reflux trichloromethane sulfenyl chloride, sulfur and catalytic amount of triethyl phosphate, as shown in scheme 2