of in situ generated arynes with vinyl sulfides provides benzannulated sulfonium ylides in a (3+2) cycloaddition. Trapping of the intermediate ylides with electrophiles (proton transfer or a second aryne addition) and subsequent β‐elimination give rise to di‐, tri‐, or tetrasubstituted alkenes with high stereoselectivity. Experimental studies and DFT calculations provide insight into the mechanisms of
Nucleophilic attack of 2-sulfinyl acrylates: A mild and general approach to sulfenic acid anions
作者:Suneel P. Singh、Jennifer S. O'Donnell、Adrian L. Schwan
DOI:10.1039/b917217c
日期:——
An increasing number of reactions of sulfenic acidanions are being demonstrated in the literature. As such, mild, general and reliable means for the generation of sulfenates are due. In the current paper, an addition/elimination of 2-sulfinyl acrylates using various nucleophiles is demonstrated and evaluated as a protocol for alkane- and arenesulfenate generation. Cyclohexanethiolate, methoxide and