| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5227624 | Tetrahedron | 2007 | 7 Pages |
Abstract
A biomimetic total synthesis of the fungal metabolite marcfortine C utilizing an intramolecular Diels-Alder reaction is described. In addition, a key stereoselective oxaziridine-mediated oxidation/pinacol rearrangement of indole 24 was used to complete the total synthesis.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Thomas J. Greshock, Alan W. Grubbs, Robert M. Williams,