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dc.contributor.authorD’Angelo, Kyan A
dc.contributor.authorSchissel, Carly K
dc.contributor.authorPentelute, Bradley L
dc.contributor.authorMovassaghi, Mohammad
dc.date.accessioned2022-03-10T20:27:04Z
dc.date.available2022-03-10T20:27:04Z
dc.date.issued2022-02-25
dc.identifier.urihttps://hdl.handle.net/1721.1/141147
dc.description.abstract<jats:p>The natural product himastatin has an unusual homodimeric structure that presents a substantial synthetic challenge. We report the concise total synthesis of himastatin from readily accessible precursors, incorporating a final-stage dimerization strategy that was inspired by a detailed consideration of the compound’s biogenesis. Combining this approach with a modular synthesis enabled expedient access to more than a dozen designed derivatives of himastatin, including synthetic probes that provide insight into its antibiotic activity.</jats:p>en_US
dc.language.isoen
dc.publisherAmerican Association for the Advancement of Science (AAAS)en_US
dc.relation.isversionof10.1126/science.abm6509en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcechemRxiven_US
dc.titleTotal synthesis of himastatinen_US
dc.typeArticleen_US
dc.identifier.citationD’Angelo, Kyan A, Schissel, Carly K, Pentelute, Bradley L and Movassaghi, Mohammad. 2022. "Total synthesis of himastatin." Science, 375 (6583).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.relation.journalScienceen_US
dc.eprint.versionOriginal manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/NonPeerRevieweden_US
dc.date.updated2022-03-10T20:22:32Z
dspace.orderedauthorsD’Angelo, KA; Schissel, CK; Pentelute, BL; Movassaghi, Men_US
dspace.date.submission2022-03-10T20:22:35Z
mit.journal.volume375en_US
mit.journal.issue6583en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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