Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5268066 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
ABC and EF ring fragments of spirolucidine have been prepared via asymmetric synthesis using chiral N-acylpyridinium salt chemistry. Model studies have been carried out to support further progress toward the completion of this complex alkaloid.
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