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Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/108043
Stereoselectivesynthesis of (-)-lepadins A-C
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A concise synthesis of the marine alkaloids ()-lepadins A-C from a phenylglycinol-derived tricyclic lactam is reported. Key steps from the stereochemical standpoint involve stereoselective cyclocondensation, double bond hydrogenation, oxazolidine opening, hydroboration- oxidation, and Horner-Wadsworth-Emmons reactions.
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AMAT TUSÓN, Mercedes, et al. Stereoselectivesynthesis of (-)-lepadins A-C. Chemical Communications. 2013. Vol. 49, num. 94, pags. 11032-11034. ISSN 1359-7345. [consulted: 5 of October of 2026]. Available at: https://hdl.handle.net/2445/108043