First Approach to the Frondosin C Ring System via a Tandem Cyclization/Claisen Rearrangement Sequence
Author:
Affiliation:
1. Department of Chemistry, Connecticut College, 270 Mohegan Avenue, New London, Connecticut 06320
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol050144o
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1. Frondosins, five new sesquiterpene hydroquinone derivatives with novel skeletons from the sponge Dysidea frondosa: Inhibitors of interleukin-8 receptors
2. (-)-Frondosins A and D, HIV-Inhibitory Sesquiterpene Hydroquinone Derivatives fromEuryspongiasp
3. From the Laboratory to the Clinic: A Retrospective on Fully Synthetic Carbohydrate-Based Anticancer Vaccines
4. Total Synthesis and Determination of the Absolute Configuration of Frondosin B
5. Concise Total Synthesis of (−)-Frondosin B Using a Novel Palladium-Catalyzed Cyclization
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