Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-9314
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dc.contributor.authorLinden, Martin-
dc.contributor.authorHofmann, Silja-
dc.contributor.authorHerman, Antonia-
dc.contributor.authorEhler, Nicole-
dc.contributor.authorBär, Robin M.-
dc.contributor.authorWaldvogel, Siegfried R.-
dc.date.accessioned2023-08-03T08:24:41Z-
dc.date.available2023-08-03T08:24:41Z-
dc.date.issued2023-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/9332-
dc.description.abstractPyrazolines and pyrazoles are common and important motifs of pharmaceutical agents and agrochemicals. Herein, the first electrochemical approach for their direct synthesis from easily accessible hydrazones and dipolarophiles up to decagram scale is presented. The application of a biphasic system (aqueous/organic) even allows for the conversion of highly sensitive alkenes, wherein inexpensive sodium iodide is employed in a dual role as supporting electrolyte and mediator. In addition, mechanistic insight into the reaction is given by the isolation of key step intermediates. The relevance of the presented reaction is underlined by the synthesis of commercial herbicide safener mefenpyr-diethyl in good yields.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.titleElectrochemical synthesis of pyrazolines and pyrazoles via [3+2] dipolar cycloadditionen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-9314-
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.titleAngewandte Chemie : international editionde
jgu.journal.volume62de
jgu.journal.issue9de
jgu.pages.alternativee202214820de
jgu.publisher.year2023-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheimde
jgu.publisher.issn1521-3773de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/anie.202214820de
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.relation.IsVersionOf10.25358/openscience-10134-
Appears in collections:DFG-491381577-H

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