Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101581
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorLam, SMen_US
dc.creatorWong, WTen_US
dc.creatorChiu, Pen_US
dc.date.accessioned2023-09-18T07:31:17Z-
dc.date.available2023-09-18T07:31:17Z-
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10397/101581-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2017 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.7b01988.en_US
dc.titleAn approach to the welwistatin core via a diazoketone rearrangement–ring expansion strategyen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage4468en_US
dc.identifier.epage4471en_US
dc.identifier.volume19en_US
dc.identifier.issue17en_US
dc.identifier.doi10.1021/acs.orglett.7b01988en_US
dcterms.abstractThe rhodium-catalyzed decomposition of fused bicyclic α-diazo-β-hydroxyketone 16 and rearrangement to 17 is featured in an approach to the bridged bicyclic core of welwistatin. The bicyclic [4.3.1] core of 25 is furnished from a subsequent cyclopropanation to generate 23, followed by its ring expansion.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOrganic letters, 1 Sept. 2017, v. 19, no. 17, p. 4468-4471en_US
dcterms.isPartOfOrganic lettersen_US
dcterms.issued2017-09-01-
dc.identifier.scopus2-s2.0-85028749489-
dc.identifier.pmid28829148-
dc.identifier.eissn1523-7052en_US
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0620-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe University of Hong Kong, the State Key Laboratory of Synthetic Chemistryen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS50634519-
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
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