Stereocontrolled Total Synthesis of (−)-Callipeltoside A
Author:
Affiliation:
1. University Chemical Laboratory, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, UK
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0357853
Reference25 articles.
1. Callipeltoside A: A Cytotoxic Aminodeoxy Sugar-Containing Macrolide of a New Type from the Marine Lithistida Sponge Callipelta sp.
2. Callipeltoside A: Total Synthesis, Assignment of the Absolute and Relative Configuration, and Evaluation of Synthetic Analogues
3. Callipeltoside A: Assignment of Absolute and Relative Configuration by Total Synthesis We thank the National Science Foundation and the National Institutes of Health for their generous support of our programs. OD was supported in part by a fellowship from the Association pour la Recherche contre le Cancer (ARC). J.L.G. was supported in part by a NIH postdoctoral fellowship from the National Cancer Institute. Mass spectra were provided by the Mass Spectroscopy Facility at the University of California, San Francisco supported by the NIH Division of Research Resources, and the Mass Spectrometry Facility at University of California, Irvine. We thank Dr. John Greaves of the latter facility for his assistance.
4. Total Synthesis of Deschlorocallipeltoside A
5. Enantioselective Total Synthesis of Callipeltoside A
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