Cu/Pd-catalyzed borocarbonylative trifunctionalization of alkynes and allenes: synthesis of β-geminal-diboryl ketones

dc.bibliographicCitation.firstPage2142eng
dc.bibliographicCitation.issue12eng
dc.bibliographicCitation.journalTitleScience China = Scientia Sinica : Chemistryeng
dc.bibliographicCitation.lastPage2153eng
dc.bibliographicCitation.volume64eng
dc.contributor.authorYuan, Yang
dc.contributor.authorWu, Fu-Peng
dc.contributor.authorSpannenberg, Anke
dc.contributor.authorWu, Xiao-Feng
dc.date.accessioned2022-04-14T08:55:27Z
dc.date.available2022-04-14T08:55:27Z
dc.date.issued2021
dc.description.abstractFunctionalized bisboryl compounds have recently emerged as a new class of synthetically useful building blocks in organic synthesis. Herein, we report an efficient strategy to synthesize β-geminal-diboryl ketones enabled by a Cu/Pd-catalyzed borocarbonylative trifunctionalization of readily available alkynes and allenes. This reaction promises to be a useful method for the synthesis of functionalized β-geminal-diboryl ketones with broad functional group tolerance. Mechanistic studies suggest that the reaction proceeds through borocarbonylation/hydroboration cascade of both alkynes and allenes.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/8698
dc.identifier.urihttps://doi.org/10.34657/7736
dc.language.isoengeng
dc.publisherBeijing : Science China Presseng
dc.relation.doihttps://doi.org/10.1007/s11426-021-1054-4
dc.relation.essn1869-1870
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc540eng
dc.subject.otheralkynes/alleneseng
dc.subject.othercarbonylationeng
dc.subject.othercopper/palladiumeng
dc.subject.othertrifunctionalizationeng
dc.subject.otherβ-geminal-diboryl ketoneseng
dc.titleCu/Pd-catalyzed borocarbonylative trifunctionalization of alkynes and allenes: synthesis of β-geminal-diboryl ketoneseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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