Electrochemical synthesis of carbazoles by dehydrogenative coupling reaction

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dc.contributor.authorKehl, Anton
dc.contributor.authorSchupp, Niclas
dc.contributor.authorBreising, Valentina M.
dc.contributor.authorSchollmeyer, Dieter
dc.contributor.authorWaldvogel, Siegfried R.
dc.date.accessioned2021-07-06T08:26:58Z
dc.date.available2021-07-06T08:26:58Z
dc.date.issued2020
dc.description.abstractA constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N-protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.en_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-6178
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/6187
dc.language.isoeng
dc.rightsCC-BY-NC-ND-4.0
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleElectrochemical synthesis of carbazoles by dehydrogenative coupling reactionen_GB
dc.typeZeitschriftenaufsatzde_DE
jgu.apc.pricePAR-Fee
jgu.journal.issue68
jgu.journal.titleChemistry - a European journal
jgu.journal.volume26
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de_DE
jgu.organisation.nameJohannes Gutenberg-Universität Mainzde_DE
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end15851
jgu.pages.start15847
jgu.publisher.doi10.1002/chem.202003430
jgu.publisher.issn1521-3765
jgu.publisher.nameWiley-VCH
jgu.publisher.placeWeinheim
jgu.publisher.urihttps://doi.org/10.1002/chem.202003430
jgu.publisher.year2020
jgu.rights.accessrightsopenAccessen_GB
jgu.subject.ddccode540
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTexten_GB
jgu.type.versionPublished versionen_GB

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