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Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/61727

Total synthesis of lamellarin D and analogs library

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Larnellarins are a group of marine natural products isolated from the prosobranch mollusc Lamellaria sp., the ascidian Didemnum sp., and the sponge Dendrilla Cactos. Several of them exhibit interesting biological activities. Natural as well as synthetic lamellarins should be excellent candidates for the development of new drugs due to their unique skeletal structure and their important biological activities especially as antitumor agents. Lamelarin O has been recently characterized as a topoisomerase 1-targeted anti tumor agent. A variety of synthetic approaches have been developed for this family of alkaloids. Herein we describe a new route to the synthesis of Lamellarin D, from a methyl 2-pyrrolecarboxylate. Transformation of the starting material into the scaffold, a substituted 5,6-dihydropyrrolo (2,l ­a)isoquinoline (5,6-DHPl), was afforded by N-alkylation followed by intramolecular Heck cyclization. From this scaffold the synthetic strategy is based on two sequential regioselective bromination!Suzuki cross-coupling reactions which permitted the introduction of differently substituted aryl groups on positions 1 and 2 followed by oxidation, deprotection, and lactonization.

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ÁLVAREZ DOMINGO, Mercedes, et al. Total synthesis of lamellarin D and analogs library. Electronic Journal of Natural Substances. 2006. Vol. 1, num. Special issue 1, pags. 39. ISSN 1951-6193. [consulted: 11 of June of 2026]. Available at: https://hdl.handle.net/2445/61727

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