Stereocontrolled Total Synthesis of (−)‐Aurisides A and B
Author:
Affiliation:
1. University Chemical Laboratory, Lensfield Road, Cambridge, CB2 1EW, UK, Fax: (+44) 1223‐336‐362
Publisher
Wiley
Subject
General Chemistry,Catalysis
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.200462267
Reference44 articles.
1. Aurisides A and B, Cytotoxic Macrolide Glycosides from the Japanese Sea Hare Dolabella auricularia
2. Synthesis of the Aglycon of Aurisides A and B, Cytotoxic Macrolide Glycosides of Marine Origin
3. For examples of other bioactive and structurally unique secondary metabolites isolated fromDolabella auricularia see:
4. Isolation of dolastatins 10–15 from the marine mollusc
5. Dolastatin H and Isodolastatin H, Potent Cytotoxic Peptides from the Sea Hare Dolabella auricularia: Isolation, Stereostructures, and Synthesis
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