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

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dc.citation.firstpage9203en_US
dc.citation.issueNumber32en_US
dc.citation.journalTitleAngewandte Chemieen_US
dc.citation.lastpage9208en_US
dc.citation.volumeNumber54en_US
dc.contributor.authorNicolaou, K.C.en_US
dc.contributor.authorShah, Akshay A.en_US
dc.contributor.authorKorman, Henryen_US
dc.contributor.authorKhan, Tabrezen_US
dc.contributor.authorShi, Leien_US
dc.contributor.authorWorawalai, Wisuttayaen_US
dc.contributor.authorTheodorakis, Emmanuel A.en_US
dc.contributor.orgBioScience Research Collaborativeen_US
dc.date.accessioned2016-10-21T17:01:00Zen_US
dc.date.available2016-10-21T17:01:00Zen_US
dc.date.issued2015en_US
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.en_US
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.en_US
dc.identifier.doihttp://dx.doi.org/10.1002/anie.201504337en_US
dc.identifier.urihttps://hdl.handle.net/1911/91977en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsThis is an author's peer-reviewed final manuscript, as accepted by the publisher. The published article is copyrighted by Wiley.en_US
dc.subject.keywordantibioticen_US
dc.subject.keywordnatural productsen_US
dc.subject.keywordstructural revisionen_US
dc.subject.keywordtotal synthesisen_US
dc.subject.keywordtransannular Diels-Alder reactionen_US
dc.titleTotal Synthesis and Structural Revision of Antibiotic CJ-16,264en_US
dc.typeJournal articleen_US
dc.type.dcmiTexten_US
dc.type.publicationpost-printen_US
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