Reductive Coupling of Aromatic Aldehydes and Ketones Under Electrochemical Conditions

Swaroop, Toreshettahally R. and Wang, Zi-Qiang and Li, Qian-Yu and Wang, Heng Shan (2020) Reductive Coupling of Aromatic Aldehydes and Ketones Under Electrochemical Conditions. Journal of the Electrochemical Society, 167 (4). ISSN 1945-7111

Full text not available from this repository. (Request a copy)
Official URL: https://iopscience.iop.org/article/10.1149/1945-71...

Abstract

Reductive coupling of o-substituted carbonyl compounds and m-substituted carbonyl compounds by the direct transfer of electron to carbonyl group respectively gave 1-(4-(1-hydroxy-1-phenylethyl/methyl)phenyl)ethanones/methanones and 2,3-bis(3-substitutedphenyl)butane/ethane-2,3-diols. 4-Methoxyacetophenone surprisingly gave 4-methoxybenzoic acid as oxidation product. Even acetophenone conjugated with alkyne group afforded interesting reductive addition product. Finally, imine also furnished reductively coupled diamino compound. Probable mechanisms for the formation of products is proposed. (c) 2020 The Electrochemical Society (''ECS''). Published on behalf of ECS by IOP Publishing Limited.

Item Type: Article
Subjects: C Chemical Science > Organic Chemistry
Divisions: Department of > Organic Chemistry
Depositing User: Mr Umendra uom
Date Deposited: 12 Feb 2021 05:36
Last Modified: 12 Feb 2021 05:36
URI: http://eprints.uni-mysore.ac.in/id/eprint/15636

Actions (login required)

View Item View Item