Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5274917 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
During the approach to the total synthesis of (+)-gelsemine, two novel spirocyclopentaneoxindole compounds 2 and 3 were obtained. Starting from compound 9, spirocyclopentaneoxindole 3 was efficiently and unexpectedly obtained through a Boc migration–intramolecular Michael cyclization cascade procedure. This intramolecular Michael addition strategy allows conveniently access to complex spirooxindole and spirocyclopentaneoxindole derivatives.
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