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dc.contributor.authorNguyen, Long V.
dc.contributor.authorJamison, Timothy F
dc.date.accessioned2020-10-02T12:58:29Z
dc.date.available2020-10-02T12:58:29Z
dc.date.issued2020-05
dc.date.submitted2020-04
dc.identifier.issn1523-7052
dc.identifier.urihttps://hdl.handle.net/1721.1/127790
dc.description.abstractA four-step synthesis of the dimeric pyrrole-imidazole alkaloid sceptrin is reported. The brevity of the route is based on a simple solution developed for selective assembly of the cyclobutane core of the natural product. The photochemical intermolecular [2 + 2] dimerization of a useful hymenidin surrogate enables direct entry to this enigmatic class of biologically active marine secondary metabolites. ©2020 American Chemical Society.en_US
dc.description.sponsorshipBill & Melinda Gates Foundationen_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttps://dx.doi.org/10.1021/acs.orglett.0c01381en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceACSen_US
dc.titleTotal Synthesis of (±)-Sceptrinen_US
dc.typeArticleen_US
dc.identifier.citationNguyen, Long V. and Timothy F. Jamison, "Total Synthesis of (±)-Sceptrin." Organic Letters 22, 17 (September 2020): 6698–6702 doi. 10.1021/acs.orglett.0c01381 ©2020 Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalOrganic Lettersen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-09-15T17:20:56Z
dspace.date.submission2020-09-15T17:20:59Z
mit.journal.volume22en_US
mit.journal.issue17en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusComplete


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