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Volumn 51, Issue 22, 2003, Pages 6537-6543

Monitoring Carbonyl-Amine Reaction between Pyruvic Acid and α-Amino Alcohols by FTIR Spectroscopy - A Possible Route to Amadori Products

Author keywords

Amadori product; Aminoethanol; Imine isomerization; MS MS; Pyruvic acid; Transamination

Indexed keywords

3 AMINO 1,2 PROPANEDIOL; AMINE; AMINOALCOHOL; AMINOSUGAR; CARBONYL DERIVATIVE; ETHANOLAMINE; IMINE; OXOACID; PYRUVIC ACID; PYRUVIC ACID METHYL ESTER; SCHIFF BASE; SOLVENT; UNCLASSIFIED DRUG;

EID: 0346363390     PISSN: 00218561     EISSN: None     Source Type: Journal    
DOI: 10.1021/jf034581y     Document Type: Article
Times cited : (42)

References (7)
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  • 5
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    • The role of β-hydroxyamino acids in the Maillard reaction-transamination route to Amadori products
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    • Yaylayan, V.; Wnorowski, A. The role of β-hydroxyamino acids in the Maillard reaction-transamination route to Amadori products. In Maillard Reaction in Food Chemistry and Medical Sciences: Update for the Postgenomic Era; Horiuchi, S., Taniguchi, N., Hayase, F., Kurata, T., and Osawa, T., Eds.; International Congress Series 1245; Elsevier Science: Amsterdam, The Netherlands, 2002; pp 195-200.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.