Please use this identifier to cite or link to this item: https://oar.tib.eu/jspui/handle/123456789/4882
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dc.rights.licenseCC BY-NC-ND 4.0 Unportedger
dc.contributor.authorPeng, J.-B.-
dc.contributor.authorWu, F.-P.-
dc.contributor.authorXu, C.-
dc.contributor.authorQi, X.-
dc.contributor.authorYing, J.-
dc.contributor.authorWu, X.-F.-
dc.date.accessioned2020-07-13T11:01:16Z-
dc.date.available2020-07-13T11:01:16Z-
dc.date.issued2018-
dc.identifier.urihttp://dx.doi.org/10.34657/3511-
dc.identifier.urihttps://oar.tib.eu/jspui/handle/123456789/4882
dc.description.abstractChemistry; Catalysis; Organic Synthesis © 2018 The Author(s)Functionalized alkyl iodides are important compounds in organic chemistry and biology. In this communication, we developed an interesting nickel-catalyzed carbonylative synthesis of functionalized alkyl iodides from aryl iodides and ethers. With Mo(CO)6 as the solid CO source, both cyclic and acyclic ethers were activated, which is also a challenging topic in organic synthesis. Functionalized alkyl iodides were prepared in moderate to excellent yields with outstanding functional group tolerance. Besides the high value of the obtained products, all the atoms from the starting materials were incorporated in the final products and the reaction had high atom efficiency as well.eng
dc.description.sponsorshipLeibniz_Fonds-
dc.language.isoeng-
dc.publisherAmsterdam : Elsevier B.V.-
dc.relation.ispartofseriesiScience Vol. 8 (2018)-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/ger
dc.subjectCatalysiseng
dc.subjectChemistryeng
dc.subjectOrganic Synthesiseng
dc.subject.ddc540-
dc.titleNickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodideseng
dc.typearticle-
dc.typeText-
dc.description.versionpublishedVersioneng
local.accessRightsopenAccess-
wgl.contributorLIKATger
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
dc.bibliographicCitation.firstPage175-
dc.bibliographicCitation.lastPage182-
dc.bibliographicCitation.volume8-
dc.relation.doihttps://doi.org/10.1016/j.isci.2018.09.024-
dc.relation.issn2589-0042-
dcterms.bibliographicCitation.journalTitleiScience-
local.identifier.doihttp://dx.doi.org/10.34657/3511-
Appears in Collections:Chemie



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