| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5223214 | Tetrahedron | 2010 | 14 Pages |
Abstract
The synthetic versatility of three chemoenzymatically prepared hydroxypiperidine building blocks has been explored, resulting in a library of enantiopure functionalized piperidines. Key steps involved N-acyliminium ion-mediated CC-bond formation and cross-metathesis reactions, after which full deprotection led to the set of free 3-hydroxypiperidines.
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