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Concise, Biomimetic Total Synthesis of d,l-Marcfortine C
Thomas J Greshock1, Alan W Grubbs, Robert M Williams
1Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523.
Tetrahedron
|July 4, 2008
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.

