Literature DB >> 2330759

Formation of acids, lactones and esters through the Maillard reaction.

J Beck1, F Ledl, M Sengl, T Severin.   

Abstract

From a glucose/glycine reaction mixture acids, esters and lactones were isolated and identified. Sugar degradation products could also be determined as benzimidazole derivatives after reaction with o-phenylenediamine. Results derived from model systems suggested possible reaction pathways leading to some of the isolated substances. A lactic acid ester is formed as a product of an unstable beta-pyranone intermediate. A 3-deoxyhexosone serves as a precursor of two furanolactones.

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Year:  1990        PMID: 2330759     DOI: 10.1007/bf01192968

Source DB:  PubMed          Journal:  Z Lebensm Unters Forsch        ISSN: 0044-3026


  3 in total

Review 1.  [The decomposition of reducing sugars and amines in the Maillard reaction].

Authors:  F Ledl
Journal:  Z Ernahrungswiss       Date:  1991-02

2.  Ribose-induced Maillard Reaction as an Analytical Method for Detection of Adulteration and Differentiation of Chilled and Frozen-thawed Minced Veal.

Authors:  Masoumeh Akbarabadi; Mohammad Mohsenzadeh; Mohammad-Reza Housaindokht
Journal:  Food Sci Anim Resour       Date:  2020-04-30

3.  Effect of hydroxyl on antioxidant properties of 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one to scavenge free radicals.

Authors:  Zhifei Chen; Qiang Liu; Zhiwei Zhao; Bing Bai; Zhitao Sun; Lili Cai; Yufeng Fu; Yuping Ma; Qingfu Wang; Gaolei Xi
Journal:  RSC Adv       Date:  2021-10-25       Impact factor: 4.036

  3 in total

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