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BEGIN:VEVENT
UID:20251102T123324EST-0361N1cT5r@132.216.98.100
DTSTAMP:20251102T173324Z
DESCRIPTION:PhD Oral Defense of Paula Vanessa Guerra Quiroz\, Department of
  Food Science and Agricultural Chemistry\nThe interaction of carbonyl moie
 ties with free amino groups initiates one of the most important chemical t
 ransformations in food\, the Maillard reaction. Among the most reactive st
 ructures produced in this reaction\, the 1\,2-dicarbonyl moieties have a s
 pecial role interacting with amino acids through the Strecker reaction to 
 generate α-amino carbonyls\, aldehydes and heterocyclic compounds\, many o
 f them aroma-active. Numerous studies have shown the interaction of a sing
 le amino acid with a 1\,2-dicarbonyl moiety\, however no systematic studie
 s have been reported on the ability of these α-dicarbonyls to undergo mult
 iple addition reactions with amino acids\, the type of products generated\
 , or alternative routes for their generation. The identification of other 
 pathways generating similar products could be considered valuable methods 
 of introducing them into the heated foods\, while the understanding of mul
 tiple addition reactions may provide a better insight into detailed chemic
 al transformations occurring in food.\n\nEveryone in the 9IÖÆ×÷³§Ãâ·Ñ community 
 is welcome to attend a PhD oral defense. Please join us in celebrating the
  accomplishments of our PhD candidates.
DTSTART:20140731T131500Z
DTEND:20140731T131500Z
LOCATION:MS2-022\, Macdonald-Stewart Building\, CA\, QC\, St Anne de Bellev
 ue\, H9X 3V9\, 21111 Lakeshore Road
SUMMARY:PhD Oral Defense: Application of Mass Spectrometry and Isotope Labe
 lling Technique to Study the Role of Various Derivatives of Α-Dicarbonyl M
 oiety in the Generation of Strecker and Maillard Reaction Products
URL:/macdonald/channels/event/phd-oral-defense-applica
 tion-mass-spectrometry-and-isotope-labelling-technique-study-role-various-
 237648
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