Total Synthesis and Structural Revision of Antibiotic CJ-16,264

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dc.citation.firstpage9203
dc.citation.issueNumber32
dc.citation.journalTitleAngewandte Chemie
dc.citation.lastpage9208
dc.citation.volumeNumber54
dc.contributor.authorNicolaou, K.C.
dc.contributor.authorShah, Akshay A.
dc.contributor.authorKorman, Henry
dc.contributor.authorKhan, Tabrez
dc.contributor.authorShi, Lei
dc.contributor.authorWorawalai, Wisuttaya
dc.contributor.authorTheodorakis, Emmanuel A.
dc.contributor.orgBioScience Research Collaborative
dc.date.accessioned2016-10-21T17:01:00Z
dc.date.available2016-10-21T17:01:00Z
dc.date.issued2015
dc.description.abstractThe total synthesis and structural revision of antibiotic CJ-16,264 is described. Starting with citronellal, the quest for the target molecule featured a novel bis-transannular Diels-Alder reaction that casted stereoselectively the decalin system and included the synthesis of six isomers before demystification of its true structure.
dc.identifier.citationNicolaou, K.C., Shah, Akshay A., Korman, Henry, et al.. "Total Synthesis and Structural Revision of Antibiotic CJ-16,264." <i>Angewandte Chemie,</i> 54, no. 32 (2015) Wiley: 9203-9208. http://dx.doi.org/10.1002/anie.201504337.
dc.identifier.doihttp://dx.doi.org/10.1002/anie.201504337
dc.identifier.urihttps://hdl.handle.net/1911/91977
dc.language.isoeng
dc.publisherWiley
dc.rightsThis is an author's peer-reviewed final manuscript, as accepted by the publisher. The published article is copyrighted by Wiley.
dc.subject.keywordantibiotic
dc.subject.keywordnatural products
dc.subject.keywordstructural revision
dc.subject.keywordtotal synthesis
dc.subject.keywordtransannular Diels-Alder reaction
dc.titleTotal Synthesis and Structural Revision of Antibiotic CJ-16,264
dc.typeJournal article
dc.type.dcmiText
dc.type.publicationpost-print
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