A Method for Constructing the C18−C28 Dispiroacetal Moiety of Altohyrtin A
Author:
Affiliation:
1. Department of Chemistry, University of California, Berkeley, California 94720
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9701703
Reference8 articles.
1. Absolute stereostructures of altohyrtin A and its congeners, potent cytotoxic macrolides from the Okinawan marine sponge hyrtios altum
2. Altohyrtin A, a potent anti-tumor macrolide from the Okinawan marine sponge Hyrtios altum
3. The Spongistatins, Potently Cytotoxic Inhibitors of Tubulin Polymerization, Bind in a Distinct Region of the Vinca Domain
4. Bioactive marine metabolites. 48. Cinachyrolide A: a potent cytotoxic macrolide possessing two spiro ketals from marine sponge Cinachyra sp
5. A Method for Constructing the C2−C12 Dispiroacetal Moiety of Altohyrtin A
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