Synthesis of the Tetrahydrofuran Ring Part of a Marine Toxin Polycavernoside-A
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/23/11/23_11_2143/_pdf
Reference9 articles.
1. Polycavernoside A: a novel glycosidic macrolide from the red alga Polycavernosa tsudai (Gracilaria edulis)
2. Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization
3. New halogenation reagent systems useful for the mild one-step conversion of alcohols into iodides or bromides
4. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
5. Regioselective reductions of 2,3-epoxy alcohols
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1. Stereoselective Synthesis of γ-Butyrolactones Subunit of Polycavernoside A;Journal of Heterocyclic Chemistry;2018-07-03
2. Rhodophyceae (Red Algae);Encyclopedia of Marine Natural Products;2014-08-07
3. Formal Total Synthesis of the Algal Toxin (−)-Polycavernoside A;Chemistry - A European Journal;2013-02-18
4. A highly diastereoselective total synthesis of (±)-heritonin and (±)-heritol;Tetrahedron;2012-10
5. ChemInform Abstract: Synthesis of the Tetrahydrofuran Ring Part of a Marine Toxin Polycavernoside-A.;ChemInform;2010-08-18
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