Total Synthesis of (+/-)-Waihoensene

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dc.contributor.authorLee, Hongsooko
dc.contributor.authorKang, Taekko
dc.contributor.authorLee, Hee-Yoonko
dc.date.accessioned2017-08-08T06:05:35Z-
dc.date.available2017-08-08T06:05:35Z-
dc.date.created2017-07-17-
dc.date.created2017-07-17-
dc.date.created2017-07-17-
dc.date.issued2017-07-
dc.identifier.citationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.28, pp.8254 - 8257-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10203/225084-
dc.description.abstractThe first total synthesis of waihoensene, a tetracyclic diterpene containing an angular triquinane and a six-membered ring, with four contiguous quaternary carbon atoms, was achieved through the tandem cycloaddition reaction of an allenyl diazo substrate containing a six-membered ring via trimethylenemethane (TMM) diyl intermediate.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleTotal Synthesis of (+/-)-Waihoensene-
dc.typeArticle-
dc.identifier.wosid000404140900040-
dc.identifier.scopusid2-s2.0-85020434893-
dc.type.rimsART-
dc.citation.volume56-
dc.citation.issue28-
dc.citation.beginningpage8254-
dc.citation.endingpage8257-
dc.citation.publicationnameANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.identifier.doi10.1002/anie.201704492-
dc.contributor.localauthorLee, Hee-Yoon-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthornatural products-
dc.subject.keywordAuthortandem cycloaddition reaction-
dc.subject.keywordAuthortotal synthesis-
dc.subject.keywordAuthortrimethylenemethane diyl-
dc.subject.keywordAuthorwaihoensene-
dc.subject.keywordPlusTANDEM CYCLOADDITION REACTIONS-
dc.subject.keywordPlusTRIMETHYLENEMETHANE DIYLS-
dc.subject.keywordPlusCARBONYL-COMPOUNDS-
dc.subject.keywordPlusNATURAL-PRODUCTS-
dc.subject.keywordPlusDIAZO-COMPOUNDS-
dc.subject.keywordPlusRING-SYSTEM-
dc.subject.keywordPlusTRIQUINANES-
dc.subject.keywordPlusMETHYLENATION-
dc.subject.keywordPlusSTRATEGIES-
dc.subject.keywordPlusLAURENENE-
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