Tsuneo Sato, Shuji Okura, J. Otera*
1987
Citations
0
Influential Citations
27
Citations
Journal
Tetrahedron Letters
Abstract
Abstract Methoxy(phenylthio)methane undergoes electrophilic alkylation followed by nucleophilic allylation or propargylation which is dramatically changed depending on the Lewis acid employed providing a methoxy- or phenylthiomethylene 1,1-dipole synthon.