Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5268595 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
A novel magnesium iodide mediated unusual dimerization–spirocyclopropanation of bromo isomerised Morita–Baylis–Hillman adducts of isatin afforded highly functionalized 3-spirocyclopropane-2-oxindole derivatives as regioisomers in good combined yield. It has been observed that the regioselectivity is dependent on the nature of electron withdrawing group at the activated position. A plausible mechanism involving organomagnesium reagent has been proposed.
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