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The electrochemical oxidation of lignin model compounds : II. Oxidation of 3,5-dimethoxy-4-hydroxyacetophenone

✍ Scribed by Wayne E. Britton; Cornelius Steelink

Publisher: Elsevier Science
Year: 1974
Tongue: French
Weight: 166 KB
Volume: 15
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(01)91766-6

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✦ Synopsis

We have recently reported on the electrochemical oxidation of the lignin model compound, 3,5-dimethoxy-4-hydroxy-a-methylbenzyl alcohol (1). The major product from that reaction in damp acetonitrile (AN) was 3,5-dimethoxy-p-benwquinone , and was thought to arise via a mechansim involving fragmentative loss of acetaldehyde. Since this oxidation pathway was unavailable

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