Difluoroalkylative carbonylation of alkenes to access carbonyl difluoro-containing heterocycles: convenient synthesis of gemigliptin

dc.bibliographicCitation.date2023
dc.bibliographicCitation.firstPage139
dc.bibliographicCitation.issue1
dc.bibliographicCitation.journalTitleScience China Chemistryeng
dc.bibliographicCitation.lastPage146
dc.bibliographicCitation.volume66
dc.contributor.authorBao, Zhi-Peng
dc.contributor.authorZhang, Youcan
dc.contributor.authorWang, Le-Cheng
dc.contributor.authorWu, Xiao-Feng
dc.date.accessioned2023-02-10T09:22:55Z
dc.date.available2023-02-10T09:22:55Z
dc.date.issued2022
dc.description.abstractFluorinated heterocycles play a vital role in pharmaceutical and agrochemical industries. Hence, rapid and efficient construction of fluorinated heterocycles remains highly demanded. Herein, a difluoroalkylative carbonylative cyclization of unactivated alkenes and ethylene gas enabled by palladium catalysis has been developed for the first time toward the synthesis of α-carbonyl difluoro-modified glutarimides. This procedure can also be applied to the synthesis of GeMigliptin which is a medicine approved for the treatment of type 2 diabetes mellitus. [Figure not available: see fulltext.]eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/11406
dc.identifier.urihttp://dx.doi.org/10.34657/10440
dc.language.isoeng
dc.publisherBerlin ; Heidelberg : Springer
dc.relation.doihttps://doi.org/10.1007/s11426-022-1439-1
dc.relation.essn1869-1870
dc.relation.issn1674-7291
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subject.ddc540
dc.subject.othercarbonylativeeng
dc.subject.otherdifluoroalkylativeeng
dc.subject.otherethylene gaseng
dc.subject.otherheterocycleseng
dc.subject.otherunactived alkeneseng
dc.titleDifluoroalkylative carbonylation of alkenes to access carbonyl difluoro-containing heterocycles: convenient synthesis of gemigliptineng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorLIKAT
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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