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Published on: October 4, 2019
Synthetic Approach to the Core Structure of Oleandrin and Related Cardiac Glycosides with Highly Functionalized Ring
Karol Michalak1, Maja Morawiak1, Jerzy Wicha1
1Institute of Organic Chemistry, Polish Academy of Sciences , Ul. Marcina Kasprzaka 44/52, 01-224 Warsaw, Poland.
Abstract:
The first synthetic approach to the core structure of cardiac glycoside oleandrin exhibiting a potent cytotoxic activity, starting from a common androstane derivative, has been accomplished. The synthesis is focused on stereoselective transformations in the densely substituted and sterically shielded five-membered ring (steroid ring D). The developed synthesis paves a route to the synthesis of related bufadienolides, i.e., constituents of traditional drug Ch'an Su, bufotalin, and cinobufagin.
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