FTIR monitoring of oxazolidin-5-one formation and decomposition in a glycolaldehyde–phenylalanine model system by isotope labeling techniques
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference6 articles.
1. Simple Generation of Nonstabilized Azomethine Ylides through Decarboxylative Condensation of α-Amino Acids with Carbonyl Compounds via 5-Oxazolidinone Intermediates
2. An Efficient Synthesis of N-Methyl Amino Acids by Way of Intermediate 5-Oxazolidinones
3. Post-Schiff Base Chemistry of the Maillard Reaction
4. Further Insight into Thermally and pH-Induced Generation of Acrylamide from Glucose/Asparagine Model Systems
5. Monitoring Carbonyl-Amine Reaction between Pyruvic Acid and α-Amino Alcohols by FTIR SpectroscopyA Possible Route To Amadori Products
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1. Amino-Acid-Derived Oxazolidin-5-Ones as Chemical Markers for Schiff Base Formation in Glycation Reactions;Applied Sciences;2023-06-28
2. Molecular Basis for the Simultaneous Enhancement of the Aroma-Generating Capacity and Bioactivity of Maillard Reaction Precursors through Mechanochemistry;Journal of Agricultural and Food Chemistry;2022-10-13
3. Effects of frying and baking processing conditions changes on biogenic amines and volatile components in Jumbo squid (Dosidicus gigas);Applied Food Research;2022-06
4. Insight into the mechanochemistry of the Maillard reaction: degradation of Schiff bases via 5-oxazolidinone intermediate;European Food Research and Technology;2021-02-08
5. Diagnostic MS/MS fragmentation patterns for the discrimination between Schiff bases and their Amadori or Heyns rearrangement products;Carbohydrate Research;2020-05
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