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dc.creatorAjdačić, Vladimir
dc.creatorNikolić, Andrea
dc.creatorKerner, Michael
dc.creatorWipf, Peter
dc.creatorOpsenica, Igor
dc.date.accessioned2018-11-22T00:44:53Z
dc.date.available2018-11-22T00:44:53Z
dc.date.issued2018
dc.identifier.issn0936-5214
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/2192
dc.description.abstractAn improved method for the decarbonylation of aliphatic aldehydes by using a commercially available Pd/C catalyst is described. The reaction conditions are suitable for linear, cyclic, or sterically demanding substrates, as they afford the corresponding alkanes in yields of up to 99%. In addition, this Pd/C-catalyzed method exhibits good functional-group tolerance. A comparison of previously reported methods with the present one showed that the reaction conditions play a crucial role in the outcome of the reaction. The method can also be applied in a two-step reaction sequence for the synthesis of industrially important compounds.en
dc.publisherGeorg Thieme Verlag Kg, Stuttgart
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172008/RS//
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/256716/EU//
dc.rightsrestrictedAccess
dc.sourceSynlett
dc.subjectdecarbonylationen
dc.subjectaldehydesen
dc.subjectpalladium catalysisen
dc.subjectadamantineen
dc.subjectalkylated aromatic compoundsen
dc.subjectnatural productsen
dc.titleReevaluation of the Palladium/Carbon-Catalyzed Decarbonylation of Aliphatic Aldehydesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractНиколић, Aндреа; Wипф, Петер; Aјдачић, Владимир; Кернер, Мицхаел; Опсеница, Игор;
dc.citation.volume29
dc.citation.issue13
dc.citation.spage1781
dc.citation.epage1785
dc.identifier.wos000440447700024
dc.identifier.doi10.1055/s-0037-1610433
dc.citation.other29(13): 1781-1785
dc.citation.rankM22
dc.description.otherSupplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/3252]
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-85051072382
dc.identifier.rcubKon_3523


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