Enantioselective Synthesis of the C(1)–C(11) Fragment of Tedanolide C
Author:
Affiliation:
1. Department of Chemistry, The Scripps Research Institute, Scripps Florida, 130 Scripps Way, Jupiter, Florida 33458, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol303089w
Reference31 articles.
1. Tedanolide C: A Potent New 18-Membered-Ring Cytotoxic Macrolide Isolated from the Papua New Guinea Marine Sponge Ircinia sp.
2. Tedanolide: a potent cytotoxic macrolide from the Caribbean sponge Tedania ignis
3. Bioactive marine metabolites. Part 35. Cytotoxic metabolites of the marine sponge Mycale adhaerens Lambe
4. Candidaspongiolides, Distinctive Analogues of Tedanolide from Sponges of the Genus Candidaspongia
5. New Candidaspongiolides, Tedanolide Analogues That Selectively Inhibit Melanoma Cell Growth
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