Synthesis of Spongidine A and D and Petrosaspongiolide L Methyl Ester Using Pyridine C–H Functionalization
Author:
Affiliation:
1. Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustraße 3, 14195 Berlin, Germany
2. Institute of Chemistry and Biochemistry, Freie Universität Berlin, Fabeckstraße 34-36, 14195 Berlin, Germany
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b04315
Reference39 articles.
1. New Pyridinium Alkaloids from a Marine Sponge of the Genus Spongia with a Human Phospholipase A2 Inhibitor Profile
2. Phospholipase A2 Enzymes: Physical Structure, Biological Function, Disease Implication, Chemical Inhibition, and Therapeutic Intervention
3. New cytotoxic sesterterpenes from the New Caledonian marine sponge Petrosaspongia nigra (Bergquist)
4. Attempted Synthesis of Spongidines by a Radical Cascade Terminating onto a Pyridine Ring
5. Zou, Y. Applications of [2+2+2] Cyclotrimerization Reactions and Light-Cleavable Groups in the Generation of Biologically Active Molecules. Dissertation, North Carolina State University, Raleigh, NC, United States, 2012.
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