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Volumn 1126, Issue , 2008, Pages 216-219

Approaches to wine aroma: C1 transfer during the reaction between diacetyl and cysteine

Author keywords

Cysteine; Diacetyl; Trimethylpyrazine; Winemaking conditions

Indexed keywords

2,3 BUTANEDIONE; PYRAZINE DERIVATIVE; TRIMETHYLPYRAZINE;

EID: 42549130327     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1196/annals.1433.023     Document Type: Conference Paper
Times cited : (4)

References (14)
  • 1
    • 0033804379 scopus 로고    scopus 로고
    • Formation of flavor compounds by the reaction of amino acid and carbonyl compounds in mild conditions
    • 1 Pripis‐Nicolau, L., G. De Revel, A. Bertrand & A. Maujean. 2000. Formation of flavor compounds by the reaction of amino acid and carbonyl compounds in mild conditions. J. Agric. Food Chem. 48: 3761–3766.
    • (2000) J. Agric. Food Chem. , vol.48 , pp. 3761-3766
    • Pripis‐Nicolau, L.1    De Revel, G.2    Bertrand, A.3    Maujean, A.4
  • 2
    • 0033790025 scopus 로고    scopus 로고
    • Approaches to wine aroma: release of aroma compounds from reactions between cysteine and carbonyl compounds in wine
    • 2 Marchand, S., G. De Revel & A. Bertrand. 2000. Approaches to wine aroma: release of aroma compounds from reactions between cysteine and carbonyl compounds in wine. J. Agric. Food Chem. 48: 4890–4895.
    • (2000) J. Agric. Food Chem. , vol.48 , pp. 4890-4895
    • Marchand, S.1    De Revel, G.2    Bertrand, A.3
  • 3
    • 1942490488 scopus 로고
    • Volatile products of the reaction of sulfur‐containing amino acids with 2,3‐butanedione
    • 3 Hartman, G.J. & C.T. Ho. 1984. Volatile products of the reaction of sulfur‐containing amino acids with 2,3‐butanedione. Lebensm.-Wiss. u.-Technol. 17: 171–174.
    • (1984) Lebensm. -Wiss. u. -Technol. , vol.17 , pp. 171-174
    • Hartman, G.J.1    Ho, C.T.2
  • 4
    • 0043043904 scopus 로고
    • Formation of oxazolines and oxazoles in Strecker degradation of DL‐alanine and L‐cysteine with 2,3‐butanedione
    • 4 Ho, C.T. & G.J. Hartman. 1982. Formation of oxazolines and oxazoles in Strecker degradation of DL‐alanine and L‐cysteine with 2,3‐butanedione. J. Agric. Food Chem. 30: 793–794.
    • (1982) J. Agric. Food Chem. , vol.30 , pp. 793-794
    • Ho, C.T.1    Hartman, G.J.2
  • 5
    • 84948882698 scopus 로고
    • Generation of Swiss cheese flavor components by the reaction of amino acids with carbonyl compounds
    • 5 Griffith, R. & G. Hammond. 1988. Generation of Swiss cheese flavor components by the reaction of amino acids with carbonyl compounds. J. Dairy Sci. 72: 604–613.
    • (1988) J. Dairy Sci. , vol.72 , pp. 604-613
    • Griffith, R.1    Hammond, G.2
  • 6
    • 0009763888 scopus 로고
    • Investigations on the reaction of amino acids with α‐dicarbonyl compounds II. Volatile products of the reaction of aminoacids with diacetyl (2,3‐butanedione)
    • 6 Piloty, M. & W. Baltes. 1979. Investigations on the reaction of amino acids with α‐dicarbonyl compounds II. Volatile products of the reaction of aminoacids with diacetyl (2,3‐butanedione). Z. Lebensm. Unters. Forsch. 168: 374–380
    • (1979) Z. Lebensm. Unters. Forsch. , vol.168 , pp. 374-380
    • Piloty, M.1    Baltes, W.2
  • 7
    • 0003144766 scopus 로고
    • 3‐Methyl‐2(1H)‐pyrazinones, the asparagine‐specific Maillard products formed from asparagine and monosaccharides
    • 7 Shu, C.K. & B.M. Lawrence. 1995. 3‐Methyl‐2(1H)‐pyrazinones, the asparagine‐specific Maillard products formed from asparagine and monosaccharides. J. Agric. Food Chem. 43: 779–781.
    • (1995) J. Agric. Food Chem. , vol.43 , pp. 779-781
    • Shu, C.K.1    Lawrence, B.M.2
  • 8
    • 33845278974 scopus 로고
    • A mechanistic study of alkylpyrazine formation in a model system
    • 8 Rizzi, G.P. 1988. A mechanistic study of alkylpyrazine formation in a model system. J. Agric. Food Chem. 36: 349–352.
    • (1988) J. Agric. Food Chem. , vol.36 , pp. 349-352
    • Rizzi, G.P.1
  • 10
    • 23744460958 scopus 로고    scopus 로고
    • Oxidative pyrolysis and postpyrolytic derivatization techniques for the total analysis of Maillard model systems: investigation of control parameters of Maillard reaction pathways
    • 10 Yaylayan, V.A, L. Haffenden, F.L Chu & A. Wnorowski. 2005. Oxidative pyrolysis and postpyrolytic derivatization techniques for the total analysis of Maillard model systems: investigation of control parameters of Maillard reaction pathways. Ann. N.Y. Acad. Sci. 1043: 41–54.
    • (2005) Ann. N.Y. Acad. Sci. , vol.1043 , pp. 41-54
    • Yaylayan, V.A1    Haffenden, L.2    Chu, F.L3    Wnorowski, A.4
  • 11
    • 0000554012 scopus 로고
    • Mechanisms of formation of alkylpyrazines in the Maillard reaction
    • 11 Amrani‐Hemaimi, M., C. Cerny, & L.B. Fay. 1995. Mechanisms of formation of alkylpyrazines in the Maillard reaction. J Agric. Food Chem. 43: 2818–2882.
    • (1995) J Agric. Food Chem. , vol.43 , pp. 2818-2882
    • Amrani‐Hemaimi, M.1    Cerny, C.2    Fay, L.B.3
  • 12
    • 0001126438 scopus 로고
    • Aromatic substitution. XX. Intact and dealkylating nitration of propylated and butylated alkylbenzenes with nitronium tetrafluoroborate
    • 12 Olah, G.A. & S.J. Kuhn. 1964. Aromatic substitution. XX. Intact and dealkylating nitration of propylated and butylated alkylbenzenes with nitronium tetrafluoroborate. J. Am. Chem. Soc. 86: 1067–1070.
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 1067-1070
    • Olah, G.A.1    Kuhn, S.J.2
  • 13
    • 1842774534 scopus 로고
    • The Hantzsch reaction. I. Oxidative dealkylation of certain dihydropyridines
    • 13 Loev, B. & K.M. Snader. 1965. The Hantzsch reaction. I. Oxidative dealkylation of certain dihydropyridines. J. Org. Chem. 30: 1914–1916.
    • (1965) J. Org. Chem. , vol.30 , pp. 1914-1916
    • Loev, B.1    Snader, K.M.2
  • 14
    • 0015152864 scopus 로고
    • Equilibria for the reaction of cysteine and derivatives with formaldehyde and protons
    • 14 Kallen, R.G. 1971. Equilibria for the reaction of cysteine and derivatives with formaldehyde and protons. J. Am. Chem. Soc. 93: 6227–6235.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 6227-6235
    • Kallen, R.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.