Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/96183
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dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorLu, YSen_US
dc.creatorYu, WYen_US
dc.date.accessioned2022-11-11T07:56:53Z-
dc.date.available2022-11-11T07:56:53Z-
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://hdl.handle.net/10397/96183-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2016 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.6b00283.en_US
dc.titleCp*Rh(III)-catalyzed cross-coupling of alkyltrifluoroborate with α-diazomalonates for C(sp³)-C(sp³) bond formationen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1350en_US
dc.identifier.epage1353en_US
dc.identifier.volume18en_US
dc.identifier.issue6en_US
dc.identifier.doi10.1021/acs.orglett.6b00283en_US
dcterms.abstractA Cp∗Rh(III)-catalyzed cross-coupling of alkyltrifluoroborate with α-diazomalonates was developed; the C(sp³)-C(sp³) bond coupled products were formed in up to 97% yields. The reaction tolerates some useful functional groups, including ketone, ester, amide, ether, sulfonyl, and thiophene. Electrospray ionization mass spectrometry (ESI-MS) analysis revealed the formation of a distinct molecular species corresponding to σ-alkylrhodium(III) complexes. The successful diazo coupling reaction may be attributed to coordination of the amide group that promotes stability of the alkylrhodium(III) complex through the formation of a five-membered metallacycle.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOrganic letters, 18 Mar. 2016, v. 18, no. 6, p. 1350-1353en_US
dcterms.isPartOfOrganic lettersen_US
dcterms.issued2016-03-18-
dc.identifier.scopus2-s2.0-84961859406-
dc.identifier.eissn1523-7052en_US
dc.description.validate202211 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberRGC-B3-0059, ABCT-0779-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6630001-
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