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dc.contributor.authorChatupheeraphat, Adisak
dc.contributor.authorLiao, Hsuan-Hung
dc.contributor.authorLee, Shao-Chi
dc.contributor.authorRueping, Magnus
dc.date.accessioned2017-10-03T12:49:36Z
dc.date.available2017-10-03T12:49:36Z
dc.date.issued2017-08-07
dc.identifier.citationChatupheeraphat A, Liao H-H, Lee S-C, Rueping M (2017) Nickel-Catalyzed C–CN Bond Formation via Decarbonylative Cyanation of Esters, Amides, and Intramolecular Recombination Fragment Coupling of Acyl Cyanides. Organic Letters 19: 4255–4258. Available: http://dx.doi.org/10.1021/acs.orglett.7b01905.
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.pmid28782964
dc.identifier.doi10.1021/acs.orglett.7b01905
dc.identifier.urihttp://hdl.handle.net/10754/625724
dc.description.abstractAn efficient nickel-catalyzed decarbonylative cyanation reaction which allows the direct functional-group interconversion of readily available esters into the corresponding nitriles was developed. This reaction successfully offers access to structurally diverse nitriles with high efficiency and excellent functional-group tolerance and provides a good alternative to classical synthetic pathways from diazonium salts or organic halide compounds.
dc.publisherAmerican Chemical Society (ACS)
dc.relation.urlhttp://pubs.acs.org/doi/full/10.1021/acs.orglett.7b01905
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/full/10.1021/acs.orglett.7b01905.
dc.titleNickel-Catalyzed C–CN Bond Formation via Decarbonylative Cyanation of Esters, Amides, and Intramolecular Recombination Fragment Coupling of Acyl Cyanides
dc.typeArticle
dc.contributor.departmentPhysical Sciences and Engineering (PSE) Division
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.identifier.journalOrganic Letters
dc.eprint.versionPost-print
dc.contributor.institutionInstitute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany
kaust.personRueping, Magnus


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