An Iodide-Mediated Anodic Amide Coupling
- Publikationstyp:
- Zeitschriftenaufsatz
- Metadaten:
-
- Autoren
- Luca Marius Grossmann
- Vera Beier
- Lea Duttenhofer
- Laura Lennartz
- Till Opatz
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000858974900001&DestLinkType=FullRecord&DestApp=WOS_CPL
- DOI
- 10.1002/chem.202202725
- eISSN
- 1521-3765
- Externe Identifier
- Clarivate Analytics Document Solution ID: 4W4MD
- PubMed Identifier: 36106367
- ISSN
- 0947-6539
- Ausgabe der Veröffentlichung
- 54
- Zeitschrift
- CHEMISTRY-A EUROPEAN JOURNAL
- Artikelnummer
- ARTN e202202725
- Datum der Veröffentlichung
- 2022
- Status
- Published
- Titel
- An Iodide-Mediated Anodic Amide Coupling
- Sub types
- Editorial Material
- Ausgabe der Zeitschrift
- 28
Datenquelle: Web of Science (Lite)
- Andere Metadatenquellen:
-
- Autoren
- Luca Marius Grossmann
- Vera Beier
- Lea Duttenhofer
- Laura Lennartz
- Till Opatz
- Autoren-URL
- https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=fis-test-1&SrcAuth=WosAPI&KeyUT=WOS:000853944800001&DestLinkType=FullRecord&DestApp=WOS_CPL
- DOI
- 10.1002/chem.202201768
- eISSN
- 1521-3765
- Externe Identifier
- Clarivate Analytics Document Solution ID: 4W4MD
- PubMed Identifier: 35835720
- ISSN
- 0947-6539
- Ausgabe der Veröffentlichung
- 54
- Zeitschrift
- CHEMISTRY-A EUROPEAN JOURNAL
- Schlüsselwörter
- amides
- electrochemistry
- iodine
- peptide
- coupling
- redox condensation
- Artikelnummer
- ARTN e202201768
- Datum der Veröffentlichung
- 2022
- Status
- Published
- Titel
- An Iodide-Mediated Anodic Amide Coupling
- Sub types
- Article
- Ausgabe der Zeitschrift
- 28
Datenquelle: Web of Science (Lite)
- Abstract
- <jats:title>Abstract</jats:title><jats:p>The 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.</jats:p>
- Autoren
- Luca Marius Großmann
- Vera Beier
- Lea Duttenhofer
- Laura Lennartz
- Till Opatz
- DOI
- 10.1002/chem.202201768
- eISSN
- 1521-3765
- ISSN
- 0947-6539
- Ausgabe der Veröffentlichung
- 54
- Zeitschrift
- Chemistry – A European Journal
- Sprache
- en
- Online publication date
- 2022
- Datum der Veröffentlichung
- 2022
- Status
- Published
- Herausgeber
- Wiley
- Herausgeber URL
- http://dx.doi.org/10.1002/chem.202201768
- Datum der Datenerfassung
- 2023
- Titel
- An Iodide‐Mediated Anodic Amide Coupling
- Ausgabe der Zeitschrift
- 28
Datenquelle: Crossref
- Abstract
- The 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.
- Addresses
- Department of Chemistry, Johannes Gutenberg University Mainz, Duesbergweg 10-14, 55128, Mainz, Germany.
- Autoren
- Luca Marius Großmann
- Vera Beier
- Lea Duttenhofer
- Laura Lennartz
- Till Opatz
- DOI
- 10.1002/chem.202201768
- eISSN
- 1521-3765
- Externe Identifier
- PubMed Identifier: 35835720
- PubMed Central ID: PMC9804404
- Open access
- true
- ISSN
- 0947-6539
- Ausgabe der Veröffentlichung
- 54
- Zeitschrift
- Chemistry (Weinheim an der Bergstrasse, Germany)
- Schlüsselwörter
- Iodides
- Amides
- Amines
- Carboxylic Acids
- Carbodiimides
- Biological Products
- Pharmaceutical Preparations
- Indicators and Reagents
- Sprache
- eng
- Medium
- Print-Electronic
- Online publication date
- 2022
- Open access status
- Open Access
- Paginierung
- e202201768
- Datum der Veröffentlichung
- 2022
- Status
- Published
- Publisher licence
- CC BY-NC-ND
- Datum der Datenerfassung
- 2022
- Titel
- An Iodide-Mediated Anodic Amide Coupling.
- Sub types
- research-article
- Journal Article
- Ausgabe der Zeitschrift
- 28
Files
https://europepmc.org/articles/PMC9804404?pdf=render
Datenquelle: Europe PubMed Central
- Abstract
- The 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.
- Autoren
- Luca Marius Großmann
- Vera Beier
- Lea Duttenhofer
- Laura Lennartz
- Till Opatz
- Autoren-URL
- https://www.ncbi.nlm.nih.gov/pubmed/35835720
- DOI
- 10.1002/chem.202201768
- eISSN
- 1521-3765
- Externe Identifier
- PubMed Central ID: PMC9804404
- Ausgabe der Veröffentlichung
- 54
- Zeitschrift
- Chemistry
- Schlüsselwörter
- amides
- electrochemistry
- iodine
- peptide coupling
- redox condensation
- Amides
- Amines
- Biological Products
- Carbodiimides
- Carboxylic Acids
- Indicators and Reagents
- Iodides
- Pharmaceutical Preparations
- Sprache
- eng
- Country
- Germany
- Paginierung
- e202201768
- Datum der Veröffentlichung
- 2022
- Status
- Published
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2022
- Titel
- An Iodide-Mediated Anodic Amide Coupling.
- Sub types
- Journal Article
- Ausgabe der Zeitschrift
- 28
Datenquelle: PubMed
- Author's licence
- CC-BY-ND
- Autoren
- Luca Marius Großmann
- Vera Beier
- Lea Duttenhofer
- Laura Lennartz
- Till Opatz
- Hosting institution
- Universitätsbibliothek Mainz
- Sammlungen
- DFG-491381577-H
- Resource version
- Published version
- DOI
- 10.1002/chem.202201768
- Funding acknowledgements
- Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 491381577
- File(s) embargoed
- false
- Open access
- true
- ISSN
- 1521-3765
- Ausgabe der Veröffentlichung
- 54
- Zeitschrift
- Chemistry - a European journal
- Schlüsselwörter
- 540 Chemie
- 540 Chemistry and allied sciences
- Sprache
- eng
- Open access status
- Open Access
- Paginierung
- e202201768
- Datum der Veröffentlichung
- 2022
- Public URL
- https://openscience.ub.uni-mainz.de/handle/20.500.12030/8719
- Herausgeber
- Wiley-VCH
- Datum der Datenerfassung
- 2023
- Datum, an dem der Datensatz öffentlich gemacht wurde
- 2023
- Zugang
- Public
- Titel
- An iodide-mediated anodic amide coupling
- Ausgabe der Zeitschrift
- 28
Files
an_iodidemediated_anodic_amid-20230127164725437.pdf
Datenquelle: OPENSCIENCE.UB
- Beziehungen:
- Eigentum von