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Nour-Eddine Es-Safi

Researcher at École Normale Supérieure

Publications -  70
Citations -  2485

Nour-Eddine Es-Safi is an academic researcher from École Normale Supérieure. The author has contributed to research in topics: Flavonols & Mass spectrometry. The author has an hindex of 27, co-authored 70 publications receiving 2241 citations. Previous affiliations of Nour-Eddine Es-Safi include Arts et Métiers ParisTech & Institut national de la recherche agronomique.

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Studies on the acetaldehyde-induced condensation of (-)-epicatechin and malvidin 3-O-glucoside in a model solution system.

TL;DR: Thioacidolysis of the two isolated anthocyanin-ethyl-flavanol dimeric derivatives showed that AnthocyanIn-ethyl linkage was not sensitive to such reactants, whereas the flavanol-ethyl one was, and flavanol's-ethyl linkages were found to be less sensitive to those involved in flavan-ethyl dimers.
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Study of the acetaldehyde induced polymerisation of flavan-3-ols by liquid chromatography-ion spray mass spectrometry

TL;DR: In this article, an on-line coupling of liquid chromatography with ion spray mass spectrometry (LC-ISP-MS) was used to identify tannin polymers.
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Study of the reactions between (+)-catechin and furfural derivatives in the presence or absence of anthocyanins and their implication in food color change.

TL;DR: (+)-catechin was separately incubated with furfural or with 5-(Hydroxymethyl)furfural, and the formation of new oligomeric bridged compounds having flavanol units linked by furfuryl or 5-hydroxymethylfurfural groups was observed, showing thus that the two polyphenols competed in the condensation process.
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Characterization of Flavonoid Glycosides from Fenugreek (Trigonella foenum-graecum) Crude Seeds by HPLC–DAD–ESI/MS Analysis

TL;DR: The quantitative analysis of the identified compounds showed that the phenolic composition of the studied crude fenugreek seeds was predominantly acylated and non-acylated flavone derivatives with apigenin as the main aglycon.
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Flavonoids: hemisynthesis, reactivity, characterization and free radical scavenging activity.

TL;DR: An overview of the findings concerning the hemisynthesis, the reactivity and the enzymatic oxidation of some flavonoids and shed light on the mechanisms involved in some of these processes and the structures of the resulting products is shed.