Synthesis of the Tetrahydropyran 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_2147/_pdf
Reference12 articles.
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4. Further synthetic studies on rifamycin s
5. Synthetic studies on polypropionate antibiotics based on the stereospecific methylation of γ δ-epoxy acrylates by trimethylaluminum. A highly stereoselective construction of the eight contiguous chiral centers of ansa-chains of rifamycins
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1. Marine-Derived Macrolides 1990–2020: An Overview of Chemical and Biological Diversity;Marine Drugs;2021-03-25
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. Asymmetric synthesis of the C(6–18) bis(tetrahydropyran)spiroacetal fragment of the lituarines;Tetrahedron;2011-07
5. ChemInform Abstract: Synthesis of the Tetrahydropyran Ring Part of a Marine Toxin Polycavernoside-A.;ChemInform;2010-08-18
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