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Volumn 1245, Issue C, 2002, Pages 195-200

The role of β-hydroxyamino acids in the Maillard reaction—transamination route to Amadori products

Author keywords

Amadori product; Amino ethanol; Imine isomerization; Pyruvic acid; Transamination

Indexed keywords


EID: 0013234654     PISSN: 05315131     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0531-5131(02)01008-7     Document Type: Article
Times cited : (8)

References (7)
  • 1
    • 0031040322 scopus 로고    scopus 로고
    • Classification of the Maillard reaction: a conceptual approach
    • Yaylayan, V.A., Classification of the Maillard reaction: a conceptual approach. Trends Food Sci. Technol. 8 (1997), 13–18.
    • (1997) Trends Food Sci. Technol. , vol.8 , pp. 13-18
    • Yaylayan, V.A.1
  • 2
    • 0001128388 scopus 로고    scopus 로고
    • Elucidation of the mechanism of pyrazinone formation in glycine model systems using labeled sugars and amino acids
    • Keyhani, A., Yaylayan, V.A., Elucidation of the mechanism of pyrazinone formation in glycine model systems using labeled sugars and amino acids. J. Agric. Food Chem. 44 (1996), 2511–2516.
    • (1996) J. Agric. Food Chem. , vol.44 , pp. 2511-2516
    • Keyhani, A.1    Yaylayan, V.A.2
  • 6
    • 0001200092 scopus 로고    scopus 로고
    • Efficient transamination under mild conditions: preparation of primary amine derivatives from carbonyl compounds via imine isomerization with catalytic amounts of potassium tert-butoxide
    • Cainelli, G., Giacomini, D., Trerè, A., Boyle, P.P., Efficient transamination under mild conditions: preparation of primary amine derivatives from carbonyl compounds via imine isomerization with catalytic amounts of potassium tert-butoxide. J. Org. Chem. 61 (1996), 5134–5139.
    • (1996) J. Org. Chem. , vol.61 , pp. 5134-5139
    • Cainelli, G.1    Giacomini, D.2    Trerè, A.3    Boyle, P.P.4
  • 7
    • 33947334511 scopus 로고
    • Electrophilic substitution at saturated carbon: XXVII. Carbanions as intermediates in the base-catalyzed methylene–azomethine rearrangement
    • Cram, D.J., Guthrie, R.D., Electrophilic substitution at saturated carbon: XXVII. Carbanions as intermediates in the base-catalyzed methylene–azomethine rearrangement. J. Am. Chem. Soc. 88 (1966), 5760–5765.
    • (1966) J. Am. Chem. Soc. , vol.88 , pp. 5760-5765
    • Cram, D.J.1    Guthrie, R.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.