Intramolecular cyclization of N-cyano sulfoximines by N–CN bond activation

Metal-free halogenated anhydrides promote the intramolecular cyclization of -cyano sulfoximines. Trifluoro- or trichloroacetic anhydride (TFAA or TCAA, respectively) activate the -cyano groups of -cyano sulfoximines, leading to the intramolecular cyclization of 2-benzamide--cyano sulfoximines 1. This method results in excellent yields of thiadiazinone 1-oxides 2. A full intramolecular cyclization pattern was suggested by (i) labeling experiments with C, (ii) isolating of -trifluoroacetyl sulfoximine 1ac, and (iii) confirming the generation of the intermediate 1ad by LC/MS analysis.