The preparation and the rearrangement of the first diaryl(acyloxy) sulfonylaminospiro-λ4-sulfane 1 are reported with the molecular structures of 1 and those of the product 2 determined by X-ray diffraction; this work demonstrates that the formation of the rearrangement products (2 or 4) depends on the N-substituent of the starting spiro-λ4-sulfane precursor, the sulfoxide 3 or cyclic imide 5.
|Number of pages||2|
|Journal||Journal of the Chemical Society, Chemical Communications|
|Publication status||Published - Dec 1 1995|
ASJC Scopus subject areas
- Molecular Medicine