Nickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodides

dc.bibliographicCitation.firstPage175eng
dc.bibliographicCitation.journalTitleiScienceeng
dc.bibliographicCitation.volume8eng
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.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.fondsLeibniz_Fonds
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/3511
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/4882
dc.language.isoengeng
dc.publisherAmsterdam : Elsevier B.V.eng
dc.relation.doihttps://doi.org/10.1016/j.isci.2018.09.024
dc.relation.issn2589-0042
dc.rights.licenseCC BY-NC-ND 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/eng
dc.subject.ddc540eng
dc.subject.otherCatalysiseng
dc.subject.otherChemistryeng
dc.subject.otherOrganic Synthesiseng
dc.titleNickel-Catalyzed Carbonylative Synthesis of Functionalized Alkyl Iodideseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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