Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-8703
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dc.contributor.authorGroßmann, Luca Marius-
dc.contributor.authorBeier, Vera-
dc.contributor.authorDuttenhofer, Lea-
dc.contributor.authorLennartz, Laura-
dc.contributor.authorOpatz, Till-
dc.date.accessioned2023-01-27T16:14:59Z-
dc.date.available2023-01-27T16:14:59Z-
dc.date.issued2022-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/8719-
dc.description.abstractThe ubiquity of amide bonds, present in natural products and common pharmaceuticals renders this functional group one of the most prevalent in organic chemistry. Despite its importance and a wide variety of existing methods for its formation, the latter still can be a challenge for classical activating reagents such as chloridating agents or carbodiimides. As the spent reagents often cannot be recycled, the development of more sustainable methods is highly desirable. Herein, we report an operationally simple and mild indirect electrochemical protocol to effect the condensation of carboxylic acids with amines, forming a wide variety of carboxamides.en_GB
dc.description.sponsorshipGefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577de
dc.language.isoengde
dc.rightsCC BY-ND*
dc.rights.urihttps://creativecommons.org/licenses/by-nd/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleAn iodide-mediated anodic amide couplingen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-8703-
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.volume28de
jgu.journal.issue54de
jgu.pages.alternativee202201768de
jgu.publisher.year2022-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheim-
jgu.publisher.issn1521-3765de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/chem.202201768de
jgu.organisation.rorhttps://ror.org/023b0x485-
jgu.subject.dfgNaturwissenschaftende
Appears in collections:DFG-491381577-H

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