Collective Total Synthesis of Ecklonialactones, Eiseniachlorides and Analogs
Abstract: Ecklonialactones, Eiseniachlorides, and Egregiachlorides are synthesized in living organisms via the lipoxygenase‐mediated oxidation of polyunsaturated fatty acids. Originally isolated and identified from brown seaweed (Ecklonia stolonifera, Eisenia bicyclis, and Egregia menziesii), and later replicated on milligram scale through chemical synthesis, the full biological activities of these compounds remain to be elucidated. To bridge this gap in knowledge, we propose a unified methodology to synthesize the 14‐membered macrocyclic structures of Ecklonialactones, Eiseniachlorides and analogs using a versatile and convergent approach. This study delineates the synthesis of Ecklonialactone A, B, C, D, and Eiseniachlorides A and B, as well as ent‐Ecklonialactone B, 16‐epi‐Ecklonialactone B and 12,13‐diepi‐Ecklonialactone B.
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Bibliographic citation
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Collective Total Synthesis of Ecklonialactones, Eiseniachlorides and Analogs ; day:09 ; month:07 ; year:2024 ; extent:8
Chemistry - a European journal ; (09.07.2024) (gesamt 8)
- Creator
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Guy, Alexandre
Delly, Shanice
Galano, Jean‐Marie
Durand, Thierry
Oger, Camille
- DOI
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10.1002/chem.202401632
- URN
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urn:nbn:de:101:1-2407101418299.601393046387
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:45 AM CEST
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Guy, Alexandre
- Delly, Shanice
- Galano, Jean‐Marie
- Durand, Thierry
- Oger, Camille
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