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Bronsted Acid Catalyzed Tandem Defunctionalization of Biorenewable Ferulic acid and Derivates into Bio-Catechol
Journal Contribution - Journal Article
An efficientconversionof biorenewableferulicacidintobio-catechol hasbeendeveloped.Thetransformationcomprisestwoconsecutivedefunctionalizationsof the sub-strate,that is,C@O(demethylation)andC@C(de-2-carbox-yvinylation)bondcleavage,occurringin one step.The processonlyrequiresheatingof ferulicacidwithHCl(or H2SO4)ascatalystin pressurized hot water(25088C, 50 bar N2). Theversatilityis shownon avarietyof other(biorenewable)substratesyieldingup to 84%di- (catechol, resorcinol,hydro-quinone)andtrihydroxybenzenes(pyrogallol,hydroxyqui-nol),in mostcasesjust requiringsimpleextractionas work-up.
Journal: Angewandte Chemie - International Edition
ISSN: 1433-7851
Issue: 8
Volume: 59
Pages: 3063 - 3068
Publication year:2020
BOF-keylabel:yes
IOF-keylabel:yes
BOF-publication weight:6
CSS-citation score:2
Authors from:Higher Education
Accessibility:Open
- See also: Bronsted Acid Catalyzed Tandem Defunctionalization of Biorenewable Ferulic acid and Derivates into Bio-Catechol
- See also: Bronsted acid catalyzed tandem defunctionalization of biorenewable ferulic acid and derivates into bio-catechol
- See also: Bronsted acid catalyzed tandem defunctionalization of biorenewable ferulic acid and derivates into bio-catechol