| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269798 | Tetrahedron Letters | 2014 | 5 Pages |
Abstract
Total synthesis of novel hybrid natural products, merosesquiterpenoids macrophorin A, 4′-oxomacrophorin A, and 1′-epi-craterellin A has been accomplished following a general strategy based on a sacrificial Diels–Alder–retroDiels–Alder approach to control regio- and stereoselectivity.
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