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dc.contributor.authorYue, Huifeng
dc.contributor.authorZhu, Chen
dc.contributor.authorRueping, Magnus
dc.date.accessioned2017-12-14T12:34:04Z
dc.date.available2017-12-14T12:34:04Z
dc.date.issued2018-01-05
dc.identifier.citationYue H, Zhu C, Rueping M (2017) Cross-Coupling of Sodium Sulfinates with Aryl, Heteroaryl and Vinyl Halides by Nickel/photoredox dual catalysis. Angewandte Chemie International Edition. Available: http://dx.doi.org/10.1002/anie.201711104.
dc.identifier.issn1433-7851
dc.identifier.doi10.1002/anie.201711104
dc.identifier.doi10.1002/ange.201711104
dc.identifier.urihttp://hdl.handle.net/10754/626369
dc.description.abstractAn efficient photoredox/nickel dual catalyzed sulfonylation reaction of aryl, heteroaryl, and vinyl halides has been achieved for the first time. This newly developed sulfonylation protocol provides a versatile method for the synthesis of diverse aromatic sulfones at room temperature and shows excellent functional group tolerance. The electrophilic coupling partners are not limited to aryl, heteroaryl and vinyl bromides but also less reactive aryl chlorides are suitable substrates for this transformation.
dc.description.sponsorshipH.Y. acknowledges the China Scholarship Council. The research leading to these results has received funding from the European Research Council under the European Union's Seventh Framework Programme (FP/2007-2013) / ERC Grant Agreement no. 617044 (SunCatChem).
dc.publisherWiley
dc.relation.urlhttp://onlinelibrary.wiley.com/doi/10.1002/anie.201711104/abstract
dc.rightsThis is the peer reviewed version of the following article: Cross-Coupling of Sodium Sulfinates with Aryl, Heteroaryl and Vinyl Halides by Nickel/photoredox dual catalysis, which has been published in final form at http://doi.org/10.1002/anie.201711104. This article may be used for non-commercial purposes in accordance With Wiley Terms and Conditions for self-archiving.
dc.titleCross-Coupling of Sodium Sulfinates with Aryl, Heteroaryl and Vinyl Halides by Nickel/photoredox dual catalysis
dc.typeArticle
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalAngewandte Chemie International Edition
dc.eprint.versionPost-print
dc.contributor.institutionInstitute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, D-52074 Aachen, Germany
kaust.personRueping, Magnus
refterms.dateFOA2018-12-06T00:00:00Z
dc.date.published-online2018-01-05
dc.date.published-print2018-01-26


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