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dc.contributor.authorJia, Jiaqi
dc.contributor.authorLefebvre, Quentin
dc.contributor.authorRueping, Magnus
dc.date.accessioned2020-01-26T05:37:51Z
dc.date.available2020-01-26T05:37:51Z
dc.date.issued2020
dc.date.submitted2019-11-29
dc.identifier.citationJia, J., Lefebvre, Q., & Rueping, M. (2020). Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis. Organic Chemistry Frontiers. doi:10.1039/c9qo01428d
dc.identifier.doi10.1039/c9qo01428d
dc.identifier.urihttp://hdl.handle.net/10754/661140
dc.description.abstractThe direct alkylation of imines with redox-active esters by visible light photoorganocatalysis provides a direct way for accessing α-branched secondary amines which are found in numerous bioactive molecules.
dc.publisherRoyal Society of Chemistry (RSC)
dc.relation.urlhttp://xlink.rsc.org/?DOI=C9QO01428D
dc.rightsArchived with thanks to Organic Chemistry Frontiers
dc.titleReductive coupling of imines with redox-active esters by visible light photoredox organocatalysis
dc.typeArticle
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalOrganic Chemistry Frontiers
dc.rights.embargodate2021-01-22
dc.eprint.versionPost-print
dc.contributor.institutionInstitute of Organic Chemistry
dc.contributor.institutionRWTH Aachen
dc.contributor.institutionAachen
dc.contributor.institutionGermany
kaust.personRueping, Magnus
dc.date.accepted2020-01-13
refterms.dateFOA2020-01-28T06:01:32Z


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