Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5218602 | Tetrahedron | 2013 | 15 Pages |
Abstract
A wealth of unique enantiopure polycyclic alkaloid-like scaffolds can be prepared on a multigram scale in only a few steps from a common, commercially available intermediate. The attached nitromethyl group can then be used to construct highly diverse functionalized libraries suitable for screening against biological targets of interest.
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