Tetrahedron Letters p. 6299 - 6302 (1987)
Update date:2022-08-03
Topics:
Sato, Tsuneo
Okura, Shuji
Otera, Junzo
Nozaki, Hitosi
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.
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