Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5223654 | Tetrahedron | 2010 | 5 Pages |
Abstract
A second-generation synthesis of the pentacyclic core of the cortistatins, a family of rearranged steroidal alkaloids that have recently attracted much attention, is reported. The improved sequence provides access to significant quantities of this key compound, which enabled a formal total synthesis of (±)-cortistatin A by conversion to the key Nicolaou/Hirama dienone. It is anticipated that this new, robust route to the pentacyclic core will facilitate the total synthesis of a range of natural products in the cortistatin family, as well as the construction of key structural analogs to probe the promising biological activity of these important compounds.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Eric M. Simmons, Alison R. Hardin-Narayan, Xuelei Guo, Richmond Sarpong,