Electrochemical synthesis of carbazoles by dehydrogenative coupling reaction

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.isoengde
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
jgu.journal.issue68de
jgu.journal.titleChemistry - a European journalde
jgu.journal.volume26de
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.end15851de
jgu.pages.start15847de
jgu.publisher.doi10.1002/chem.202003430
jgu.publisher.issn1521-3765de
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.urihttps://doi.org/10.1002/chem.202003430de
jgu.publisher.year2020
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode540de
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde

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