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Electrochemical deoxygenation of primary alcohols

Electrochemical deoxygenation of primary alcohols

Lam, Kevin ORCID logoORCID: https://orcid.org/0000-0003-1481-9212 and Markó, István E. (2012) Electrochemical deoxygenation of primary alcohols. Synlett, 23 (8). pp. 1235-1239. ISSN 0936-5214 (Print), 1437-2096 (Online) (doi:10.1055/s-0031-1290778)

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Abstract

Direct electrolysis of primary alcohols, in the presence of methyl toluate, leads smoothly to the formation of the corresponding deoxygenated product in high yield.

Item Type: Article
Uncontrolled Keywords: Deoxygenation, Electrochemical, Esters, Free radicals, Reduction
Subjects: Q Science > QC Physics
Q Science > QD Chemistry
Faculty / School / Research Centre / Research Group: Faculty of Engineering & Science
Faculty of Engineering & Science > School of Science (SCI)
Last Modified: 10 Oct 2017 16:22
URI: http://gala.gre.ac.uk/id/eprint/17709

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