Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1335258 | Polyhedron | 2008 | 7 Pages |
A highly regioselective method for the synthesis of β-iodohydrins and β-bromohydrins through direct ring opening of epoxides with elemental halogen in the presence of alumina-supported Schiff base complexes of Mn(II), Co(II), Ni(II) and Cu(II) as new catalysts is described. This method is regioselective under mild conditions in various aprotic solvents with high yields, even when sensitive functional groups are present. The catalysts are easily recovered and can be reused several times.
Graphical abstractA highly regioselective method for the synthesis of β-iodohydrins and β-bromohydrins by direct ring opening of epoxides with elemental halogen in the presence of alumina-supported Mn(II), Co(II), Ni(II) and Cu(II) Schiff-base complexes as new catalysts is described. This method occur regioselectively under mild conditions with high yields in various aprotic solvents, even when sensitive functional groups are present.Figure optionsDownload full-size imageDownload as PowerPoint slide