Establishing a “Ring‐Size‐Divergent” Synthetic Strategy: Synthesis, Structural Revision, and Absolute Configuration of Feroniellins
Author:
Affiliation:
1. Department of Chemistry Graduate School of Science Osaka City University Sumiyoshi-ku Osaka 558-8585 Japan
2. Faculty of Fisheries Kagoshima University Shimoarata Kagoshima 8900056 Japan
Funder
Shorai Foundation for Science and Technology
Publisher
Wiley
Subject
General Chemistry,Catalysis,Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202101603
Reference31 articles.
1. Feroniellins A–C, novel cytotoxic furanocoumarins with highly oxygenated C10 moieties from Feroniella lucida
2. Feroniellin A-induced autophagy causes apoptosis in multidrug-resistant human A549 lung cancer cells
3. Feroniellin B, A new highly potent human platelet aggregation inhibitor fromFeroniella lucida
4. A novel furanocoumarin fromFeroniella lucida exerts protective effect against lipid peroxidation
5. Epoxide-Opening Cascades in the Synthesis of Polycyclic Polyether Natural Products
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1. Gold‐catalyzed endo‐selective Ring‐opening of Epoxides and its Application in Construction of Poly‐ethers;Chemistry – A European Journal;2024-02-20
2. Establishment of “Ring-Size-Divergent” Synthetic Strategy: Divergent Synthesis, Stereochemical Assignments, and Biological Activity Studies of Nerolidol-Type Sesquiterpenoids and Feroniellins;The Journal of Organic Chemistry;2023-11-04
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