Please use this identifier to cite or link to this item:
http://doi.org/10.25358/openscience-8695
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Gombos, Lilla G. | - |
dc.contributor.author | Werner, Leo | - |
dc.contributor.author | Schollmeyer, Dieter | - |
dc.contributor.author | Martínez-Huitle, Carlos A. | - |
dc.contributor.author | Waldvogel, Siegfried R. | - |
dc.date.accessioned | 2023-01-30T10:07:11Z | - |
dc.date.available | 2023-01-30T10:07:11Z | - |
dc.date.issued | 2022 | - |
dc.identifier.uri | https://openscience.ub.uni-mainz.de/handle/20.500.12030/8711 | - |
dc.description.abstract | A simple electrochemical protocol is established for the selective alkene dibromination of naturally derived olefins, such as terpenes. The use of hazardous Br2 or its analogues have been elegantly avoided by employing readily available, inexpensive, and harmless sodium bromide with a dual role as reagent and supporting electrolyte in combination with sustainable carbon-based electrodes. This electrochemical protocol provides the desired products with good to excellent yields up to 82 % with 10 examples. Scalability has been proved by a 5-fold scale-up. Notably, higher yields and selectivity were achieved in comparison to conventional bromination by Br2 and DMSO/HBr system and the dibrominated compound was eligible for further functionalization, such as cyanation according to the Kolbe nitrile synthesis protocol. | en_GB |
dc.description.sponsorship | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577 | de |
dc.language.iso | eng | de |
dc.rights | CC BY-NC-ND | * |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject.ddc | 540 Chemie | de_DE |
dc.subject.ddc | 540 Chemistry and allied sciences | en_GB |
dc.title | Selective electrochemical dibromination of terpenes and naturally derived olefins | en_GB |
dc.type | Zeitschriftenaufsatz | de |
dc.identifier.doi | http://doi.org/10.25358/openscience-8695 | - |
jgu.type.dinitype | article | en_GB |
jgu.type.version | Published version | de |
jgu.type.resource | Text | de |
jgu.organisation.department | FB 09 Chemie, Pharmazie u. Geowissensch. | de |
jgu.organisation.number | 7950 | - |
jgu.organisation.name | Johannes Gutenberg-Universität Mainz | - |
jgu.rights.accessrights | openAccess | - |
jgu.journal.title | European journal of organic chemistry | de |
jgu.journal.volume | 2022 | de |
jgu.journal.issue | 47 | de |
jgu.pages.alternative | e202200857 | de |
jgu.publisher.year | 2022 | - |
jgu.publisher.name | Wiley VCZ | de |
jgu.publisher.place | Weinheim | - |
jgu.publisher.issn | 1099-0690 | de |
jgu.organisation.place | Mainz | - |
jgu.subject.ddccode | 540 | de |
jgu.publisher.doi | 10.1002/ejoc.202200857 | de |
jgu.organisation.ror | https://ror.org/023b0x485 | - |
jgu.subject.dfg | Naturwissenschaften | de |
Appears in collections: | DFG-491381577-H |
Files in This Item:
File | Description | Size | Format | ||
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selective_electrochemical_dib-20230130110343444.pdf | 4.01 MB | Adobe PDF | View/Open |