dc.contributor.authorKaga, Atsushi
dc.contributor.authorChiba, Shunsuke
dc.date.accessioned2019-05-16T09:13:58Z
dc.date.available2019-05-16T09:13:58Z
dc.date.issued2017
dc.identifier.citationKaga, A., & Chiba, S. (2017). Synthesis of tricyclic marine alkaloids, cylindricines, lepadiformines, fasicularin, and polycitorols : a recent update. Synthesis, 50(04), 685-699. doi:10.1055/s-0036-1589521en_US
dc.identifier.issn0039-7881en_US
dc.identifier.urihttp://hdl.handle.net/10220/48243
dc.description.abstractCylindricines, lepadiformines, and fasicularin are tricyclic marine alkaloids bearing perhydropyrrolo- and pyrido[2,1-j] frameworks having divergent chemical functionalities. They have been isolated from marine tunicates over the last two decades and found to have a range of cytotoxicity such as DNA-alkylating ability. Recently, polycitorols have emerged as a new member of this alkaloid family. Their unique structural features and biological activities have intrigued many researchers and challenged them in their synthesis. This review describes recent syntheses of the tricyclic alkaloids based on key synthetic approaches.en_US
dc.description.sponsorshipMOE (Min. of Education, S’pore)en_US
dc.format.extent14 p.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesSynthesisen_US
dc.rights© 2018 Thieme Publishing. All rights reserved. This paper was published in Synthesis and is made available with permission of Thieme Publishing.en_US
dc.subjectTricyclic Alkaloidsen_US
dc.subjectNatural Productsen_US
dc.subjectDRNTU::Science::Chemistryen_US
dc.titleSynthesis of tricyclic marine alkaloids, cylindricines, lepadiformines, fasicularin, and polycitorols : a recent updateen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1055/s-0036-1589521
dc.description.versionAccepted versionen_US


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