Green Chem., 2026, Advance Article
DOI: 10.1039/D5GC05640C, Paper
DOI: 10.1039/D5GC05640C, Paper
Open Access
  This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.Julius Ponhöfer, Moritz Lukas Krebs, Ferdi Schüth
Acetalization of 5-hydroxymethylfurfural shifts selectivity during alkaline electrooxidation toward 5-formyl-2-furancarboxylic acid. This protective strategy prevents humin formation and enables high yields and efficiency under harsh conditions.
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Acetalization of 5-hydroxymethylfurfural shifts selectivity during alkaline electrooxidation toward 5-formyl-2-furancarboxylic acid. This protective strategy prevents humin formation and enables high yields and efficiency under harsh conditions.
To cite this article before page numbers are assigned, use the DOI form of citation above.
The content of this RSS Feed (c) The Royal Society of Chemistry
