Synthesis and stereochemical confirmation of the cis-fused L/M and N/O ring systems of maitotoxin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Toxicity of the surgeonfishes. II. Properties of the principal water-soluble toxin.
2. Partial structures of maitotoxin, the most potent marine toxin from the dinoflagellate Gambierdiscus toxicus
3. Structure of maitotoxin
4. Isolation and structure of brevetoxin B from the "red tide" dinoflagellate Ptychodiscus brevis (Gymnodinium breve)
5. Structure of brevetoxin A (GB-1 toxin), the most potent toxin in the Florida red tide organism Gymnodinium breve (Ptychodiscus brevis)
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1. Scalable synthesis of the L/N ring of maitotoxin;Tetrahedron Letters;2024-09
2. Synthesis of the WXYZA'B'C'D'E'F' Ring of Maitotoxin;Journal of Synthetic Organic Chemistry, Japan;2023-01-01
3. Convergent Synthesis of the WXYZA′B′C′D′E′F′ Ring Segment of Maitotoxin;Bulletin of the Chemical Society of Japan;2022-02-15
4. Synthesis-Driven Stereochemical Assignment of Marine Polycyclic Ether Natural Products;Marine Drugs;2021-04-29
5. Structure Determination, Chemical Synthesis, and Evaluation of Biological Activity of Super Carbon Chain Natural Products;Bulletin of the Chemical Society of Japan;2020-11-15
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