Convenient and General Zinc-Catalyzed Borylation of Aryl Diazonium Salts and Aryltriazenes under Mild Conditions

dc.bibliographicCitation.firstPage345
dc.bibliographicCitation.issue3
dc.bibliographicCitation.journalTitleChemistryOpeneng
dc.bibliographicCitation.lastPage349
dc.bibliographicCitation.volume6
dc.contributor.authorQi, Xinxin
dc.contributor.authorJiang, Li-Bing
dc.contributor.authorZhou, Chao
dc.contributor.authorPeng, Jin-Bao
dc.contributor.authorWu, Xiao-Feng
dc.date.accessioned2023-01-19T09:43:51Z
dc.date.available2023-01-19T09:43:51Z
dc.date.issued2017-3-16
dc.description.abstractA convenient and general zinc-catalyzed borylation of aryl diazonium salts and aryltriazenes has been developed. With bis- (pinacolato)diboron as the borylation reagent, aryldiazonium tetrafluoroborate salts and aryltriazenes were transformed into the corresponding arylboronates in moderate to excellent yields under mild conditions. As a convenient and practical methodology, no additional ligands, base, or any other additives are required here.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/10935
dc.identifier.urihttp://dx.doi.org/10.34657/9961
dc.language.isoeng
dc.publisherWeinheim : Wiley-VCH-Verl.
dc.relation.doihttps://doi.org/10.1002/open.201700036
dc.relation.essn2191-1363
dc.relation.issn2191-1355
dc.rights.licenseCC BY-NC-ND 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc540
dc.subject.otherarylboronateseng
dc.subject.otheraryldiazonium saltseng
dc.subject.otheraryltriazeneseng
dc.subject.otherborylationeng
dc.subject.otherzinc catalysiseng
dc.titleConvenient and General Zinc-Catalyzed Borylation of Aryl Diazonium Salts and Aryltriazenes under Mild Conditionseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorLIKAT
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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