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  4. Determination of 4-Hydroxy-2,5-dimethyl-3(2H)-furanone and 2(or 5)-Ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in Pentose Sugar-Based Maillard Model Systems by Isotope Dilution Assays
 
research article

Determination of 4-Hydroxy-2,5-dimethyl-3(2H)-furanone and 2(or 5)-Ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in Pentose Sugar-Based Maillard Model Systems by Isotope Dilution Assays

Blank, Imre
•
Fay, Laurent B.
•
Lakner, Frederick J.
Show more
1997
Journal of Agricultural and Food Chemistry

The formation of 4-hydroxy-2,5-dimethyl-3(2H)-furanone (HDMF) and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone (EHMF) from pentose sugars was studied in Maillard model systems. The amts. generated at 90 DegC for 1 h were detd. by isotope diln. assay (IDA). The internal stds. used for IDA, i.e., [13C2]HDMF and [2H3]EHMF, were prepd. in good overall yields in 3 steps: addn. of labeled acetaldehyde or propionaldehyde to tert-butyloxycarbonyl (BOC)-protected and lithiated 3-butyn-2-ol; oxidn. of the BOC-protected diol with permanganate to 1,2-dione; and finally cyclization to the target mols. after removal of the protective groups under acidic conditions. Quant. data confirmed previous findings that HDMF and EHMF are preferentially formed in the presence of glycine and L-alanine, resp. The yields obtained were 2.6-5.1 mg of HDMF and 6.8-10 mg of EHMF per mmol pentose. Formation of both furanones was favored in phosphate-buffered solns. at pH 7 compared to pH 5, particularly in the presence of an excess of amino acid. These data are well in agreement with the previously proposed formation mechanism of HDMF and EHMF via Strecker-assisted chain elongation of the pentose moiety. However, both furanones were also produced to a lesser extent by sugar fragmentation-condensation reactions. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1021/jf960997i
Author(s)
Blank, Imre
Fay, Laurent B.
Lakner, Frederick J.
Schlosser, Manfred  
Date Issued

1997

Published in
Journal of Agricultural and Food Chemistry
Volume

45

Issue

7

Start page

2642

End page

2648

Subjects

Oxidation (alkyne; detn. of 4-hydroxy-2

•

5-dimethyl-3(2H)-furanone and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in pentose sugar-based maillard model systems by isotope diln. assays); Isotope dilution mass spectrometry; Maillard reaction; Si

•

furanone formation detn pentose sugar Maillard

Note

CAN 127:64740 17-2 Food and Feed Chemistry Nestle Research Center,Nestec Ltd.,Lausanne,Switz. Journal 0021-8561 written in English. 27538-09-6 (3(2H)-Furanone, 5-ethyl-4-hydroxy-2-methyl-); 27538-10-9 Role: ANT (Analyte), BOC (Biological occurrence), BSU (Biological study, unclassified), MFM (Metabolic formation), ANST (Analytical study), BIOL (Biological study), FORM (Formation, nonpreparative), OCCU (Occurrence) (detn. of 4-hydroxy-2,5-dimethyl-3(2H)-furanone and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in pentose sugar-based maillard model systems by isotope diln. assays); 3658-77-3 (4-Hydroxy-2,5-dimethyl-3(2H)-furanone) Role: ANT (Analyte), BOC (Biological occurrence), BSU (Biological study, unclassified), MFM (Metabolic formation), PRP (Properties), ANST (Analytical study), BIOL (Biological study), FORM (Formation, nonpreparative), OCCU (Occurrence) (detn. of 4-hydroxy-2,5-dimethyl-3(2H)-furanone and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in pentose sugar-based maillard model systems by isotope diln. assays); 2028-63-9 (3-Butyn-2-ol); 24424-99-5 (Di-tert-butyl dicarbonate) Role: RCT (Reactant), RACT (Reactant or reagent) (detn. of 4-hydroxy-2,5-dimethyl-3(2H)-furanone and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in pentose sugar-based maillard model systems by isotope diln. assays); 191528-22-0P; 191528-23-1P; 191528-24-2P; 191528-25-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (detn. of 4-hydroxy-2,5-dimethyl-3(2H)-furanone and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in pentose sugar-based maillard model systems by isotope diln. assays); 191528-21-9P Role: SPN (Synthetic preparation), PREP (Preparation) (detn. of 4-hydroxy-2,5-dimethyl-3(2H)-furanone and 2(or 5)-ethyl-4-hydroxy-5(or 2)-methyl-3(2H)-furanone in pentose sugar-based maillard model systems by isotope diln. assays)

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Available on Infoscience
March 3, 2006
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/226941
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