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dc.contributor.authorMagre, Marc
dc.contributor.authorSzewczyk, Marcin
dc.contributor.authorRueping, Magnus
dc.date.accessioned2020-02-11T06:13:45Z
dc.date.available2020-02-11T06:13:45Z
dc.date.issued2020-02-05
dc.date.submitted2020-01-13
dc.identifier.citationMagre, M., Szewczyk, M., & Rueping, M. (2020). Magnesium-Catalyzed Stereoselective Hydrostannylation of Internal and Terminal Alkynes. Organic Letters. doi:10.1021/acs.orglett.0c00184
dc.identifier.doi10.1021/acs.orglett.0c00184
dc.identifier.urihttp://hdl.handle.net/10754/661460
dc.description.abstractA regio- and stereoselective magnesium-catalyzed hydrostannylation of internal and terminal alkynes has been developed. Excellent yields and selectivities are obtained for a wide range of terminal and internal symmetrical and unsymmetrical alkynes by using this alkaline earth metal catalyst as an effective alternative to transition metal catalysts.
dc.publisherAmerican Chemical Society (ACS)
dc.relation.urlhttps://pubs.acs.org/doi/10.1021/acs.orglett.0c00184
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 https://pubs.acs.org/doi/10.1021/acs.orglett.0c00184.
dc.titleMagnesium-Catalyzed Stereoselective Hydrostannylation of Internal and Terminal Alkynes
dc.typeArticle
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalOrganic Letters
dc.rights.embargodate2021-02-05
dc.eprint.versionPost-print
dc.contributor.institutionInstitute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074 Aachen, Germany
kaust.personRueping, Magnus
refterms.dateFOA2020-02-11T10:36:50Z
dc.date.published-online2020-02-05
dc.date.published-print2020-02-21


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