Katona ezer Póráz galacturonic acid pka Független fülke statisztika
Determination of the pKa of glucuronic acid and the carboxy groups of heparin by 13C-nuclear-magnetic-resonance spectroscopy. - Abstract - Europe PMC
D-Galacturonic acid - American Chemical Society
Dissociation constants of D-galacturonic and D-glucuronic acid and their О-methyl derivatives
Galacturonic Acid - an overview | ScienceDirect Topics
Simultaneous fermentation of galacturonic acid and five-carbon sugars by engineered Saccharomyces cerevisiae - ScienceDirect
Engineering Saccharomyces cerevisiae for co-utilization of d-galacturonic acid and d-glucose from citrus peel waste | Nature Communications
d-Galacturonic Acid: A Highly Reactive Compound in Nonenzymatic Browning. 2. Formation of Amino-Specific Degradation Products | Journal of Agricultural and Food Chemistry
What are Gluconic acid (E574) and Gluconates in Food and Uses?
Improvement of nanofibrillation efficiency of α-chitin in water by selecting acid used for surface cationisation - RSC Advances (RSC Publishing) DOI:10.1039/C2RA22271J
Galacturonic Acid - an overview | ScienceDirect Topics
Galacturonic Acid - an overview | ScienceDirect Topics
D-Galacturonic acid - Wikipedia
Engineering Filamentous Fungi for Conversion of d-Galacturonic Acid to l-Galactonic Acid | Applied and Environmental Microbiology
Pectin: The Miracle Molecule
PDF] Determination of the pKa of glucuronic acid and the carboxy groups of heparin by 13C-nuclear-magnetic-resonance spectroscopy. | Semantic Scholar
Influence of the Carboxylic Function on the Degradation of d-Galacturonic Acid and Its Polymers | Journal of Agricultural and Food Chemistry
pKa - an overview | ScienceDirect Topics
d-Galacturonic Acid: A Highly Reactive Compound in Nonenzymatic Browning. 2. Formation of Amino-Specific Degradation Products | Journal of Agricultural and Food Chemistry
d-Galacturonic Acid: A Highly Reactive Compound in Nonenzymatic Browning. 2. Formation of Amino-Specific Degradation Products | Journal of Agricultural and Food Chemistry
Anomer Preferences for Glucuronic and Galacturonic Acid and Derivatives and Influence of Electron-Withdrawing Substituents | The Journal of Organic Chemistry