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dc.contributor.authorPashikanti, Srinath
dc.contributor.authorUkani, Rehman
dc.contributor.authorDavid, Sunil A.
dc.contributor.authorDatta, Apurba
dc.date.accessioned2018-11-01T18:00:49Z
dc.date.available2018-11-01T18:00:49Z
dc.date.issued2017
dc.identifier.citationPashikanti, S., Rehnman, U., David, S. A., Apurba, D., (2017), FTotal Synthesis and Structure–Activity Relationship Studies of the Cytotoxic Anhydrophytosphingosine Jaspine B (Pachastrissamine), Synthesis, https://doi.org/10.1055/s-0036-1588118en_US
dc.identifier.urihttp://hdl.handle.net/1808/27129
dc.description.abstractBy utilizing an l-serine-derived bicyclic lactone as an advanced chiral building block, a short synthetic route to the cytotoxic marine natural product jaspine B has been developed. Targeting structure–activity relationship investigations, the synthetic route has also been utilized for the synthesis and cytotoxicity evaluation of strategically modified jaspine B analogues. In addition, a previously reported synthesis of the title natural product from our research has been reinvestigated to clarify the sterochemical assignment.en_US
dc.publisherThieme Publishingen_US
dc.subjectJaspine Ben_US
dc.subjectStereochemistryen_US
dc.subjectCytotoxicen_US
dc.subjectDrug developmenten_US
dc.subjectStructureen_US
dc.subjectActivity relationshipsen_US
dc.titleTotal Synthesis and Structure–Activity Relationship Studies of the Cytotoxic Anhydrophytosphingosine Jaspine B (Pachastrissamine)en_US
dc.typeArticleen_US
kusw.kuauthorDutta, Apurba
kusw.kudepartmentMedicinal Chemistryen_US
dc.identifier.doi10.1055/s-0036-1588118en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccessen_US


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