Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-6247
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dc.contributor.authorBlum, Stephan P.-
dc.contributor.authorSchollmeyer, Dieter-
dc.contributor.authorTurks, Maris-
dc.contributor.authorWaldvogel, Siegfried R.-
dc.date.accessioned2021-08-06T10:02:56Z-
dc.date.available2021-08-06T10:02:56Z-
dc.date.issued2020-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/6257-
dc.description.abstractThis work presents the first electrochemical preparation of alkyl arylsulfonates by direct anodic oxidation of electron-rich arenes. The reaction mechanism features a multi-component reaction consisting of electron-rich arenes, an alcohol of choice and excess SO2 in an acetonitrile-HFIP reaction mixture. In-situ formed monoalkyl sulfites are considered as key intermediates with bifunctional purpose. Firstly, this species functions as nucleophile and secondly, excellent conductivity is provided. Several primary and secondary alcohols and electron-rich arenes are implemented in this reaction to form the alkyl arylsulfonates in yields up to 73 % with exquisite selectivity. Boron-doped diamond electrodes (BDD) are employed in divided cells, separated by a simple commercially available glass frit.en_GB
dc.language.isoengde
dc.rightsCC BY-NC-ND*
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.titleMetal- and reagent-free electrochemical synthesis of alkyl arylsulfonates in a multi-component reactionen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-6247-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleChemistry - a European journalde
jgu.journal.volume26de
jgu.journal.issue38de
jgu.pages.start8358de
jgu.pages.end8362de
jgu.publisher.year2020-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.urihttps://doi.org/10.1002/chem.202001180de
jgu.publisher.issn1521-3765de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/chem.202001180
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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