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dc.contributor.authorMillet, Anthony
dc.contributor.authorLefebvre, Quentin
dc.contributor.authorRueping, Magnus
dc.date.accessioned2016-11-03T13:22:48Z
dc.date.available2016-11-03T13:22:48Z
dc.date.issued2016-06-20
dc.identifier.citationMillet A, Lefebvre Q, Rueping M (2016) Visible-Light Photoredox-Catalyzed Giese Reaction: Decarboxylative Addition of Amino Acid Derived α-Amino Radicals to Electron-Deficient Olefins. Chemistry - A European Journal 22: 13464–13468. Available: http://dx.doi.org/10.1002/chem.201602257.
dc.identifier.issn0947-6539
dc.identifier.pmid27321136
dc.identifier.doi10.1002/chem.201602257
dc.identifier.urihttp://hdl.handle.net/10754/621688
dc.description.abstractA tin- and halide-free, visible-light photoredox-catalyzed Giese reaction was developed. Primary and secondary α-amino radicals were generated readily from amino acids in the presence of catalytic amounts of an iridium photocatalyst. The reactivity of the α-amino radicals has been evaluated for the functionalization of a variety of activated olefins. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
dc.description.sponsorshipEuropean Research Council
dc.description.sponsorshipEuropean Union[617044]
dc.publisherWiley
dc.subjectamino acid
dc.subjectdecarboxylation
dc.subjectheterocycles
dc.subjectphotoredox catalysis
dc.titleVisible-Light Photoredox-Catalyzed Giese Reaction: Decarboxylative Addition of Amino Acid Derived α-Amino Radicals to Electron-Deficient Olefins
dc.typeArticle
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalChemistry - A European Journal
dc.contributor.institutionInstitute of Organic Chemistry; RWTH Aachen; Landoltweg 1 52074 Aachen Germany
kaust.personRueping, Magnus
dc.date.published-online2016-06-20
dc.date.published-print2016-09-12


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