| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276231 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
A concise, enantiodivergent formal synthesis of (+)-paecilomycine A and its antipode, involving a 1,4-chirality transfer protocol and an intramolecular Pauson–Khand reaction as the key steps is outlined.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
