Xylochemical synthesis and biological evaluation of shancigusin C and bletistrin G ‡

dc.contributor.authorGeske, Leander
dc.contributor.authorKauhl, Ulrich
dc.contributor.authorSaaed, Mohamed E. M.
dc.contributor.authorSchüffler, Anja
dc.contributor.authorThines, Eckhard
dc.contributor.authorEfferth, Thomas
dc.contributor.authorOpatz, Till
dc.date.accessioned2021-11-15T10:12:53Z
dc.date.available2021-11-15T10:12:53Z
dc.date.issued2021
dc.description.abstractThe biological activities of shancigusin C (1) and bletistrin G (2), natural products isolated from orchids, are reported along with their first total syntheses. The total synthesis of shancigusin C (1) was conducted by employing the Perkin reaction to forge the central stilbene core, whereas the synthesis of bletistrin G (2) was achieved by the Wittig olefination followed by several regioselective aromatic substitution reactions. Both syntheses were completed by applying only renewable starting materials according to the principles of xylochemistry. The cytotoxic properties of shancigusin C (1) and bletistrin G (2) against tumor cells suggest suitability as a starting point for further structural variation.en_GB
dc.description.sponsorshipOpen Access-Publizieren Universität Mainz / Universitätsmedizin Mainzde
dc.identifier.doihttp://doi.org/10.25358/openscience-6508
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/6518
dc.language.isoengde
dc.rightsCC-BY-4.0*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc570 Biowissenschaftende_DE
dc.subject.ddc570 Life sciencesen_GB
dc.titleXylochemical synthesis and biological evaluation of shancigusin C and bletistrin G ‡en_GB
dc.typeZeitschriftenaufsatzde
jgu.journal.issue11de
jgu.journal.titleMoleculesde
jgu.journal.volume26de
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternative3224de
jgu.publisher.doi10.3390/molecules26113224
jgu.publisher.issn1420-3049de
jgu.publisher.nameMDPIde
jgu.publisher.placeBaselde
jgu.publisher.urihttps://doi.org/10.3390/molecules26113224de
jgu.publisher.year2021
jgu.rights.accessrightsopenAccess
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde

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