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Volumn 70, Issue 4, 2006, Pages 958-965

Potent odorants characterize the aroma quality of leaves and stalks in raw and boiled celery

Author keywords

3 n butylphthalide; Aroma extract dilution analysis; Celery (Apium graveolens L. Var. dulce); Sedanenolide; Sedanolide

Indexed keywords

ALCOHOLS; ODORS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PLANTS (BOTANY); RAW MATERIALS;

EID: 33646132511     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.70.958     Document Type: Article
Times cited : (39)

References (20)
  • 1
    • 33646153635 scopus 로고
    • The hydrophthalides. 1. Action of magnesium iodoalkyls on δ-2-tetrahydrophthalic anhydride
    • Berlingozzi, S., and Mazzo, F. P., The hydrophthalides. 1. Action of magnesium iodoalkyls on δ-2-tetrahydrophthalic anhydride. Gazz. Chim. Ital., 56, 88-98 (1926).
    • (1926) Gazz. Chim. Ital. , vol.56 , pp. 88-98
    • Berlingozzi, S.1    Mazzo, F.P.2
  • 2
    • 0002582878 scopus 로고
    • Alkylidene phthalides and dihydrophthalides from celery
    • Gold, H. J., and Wilson, C. W., Alkylidene phthalides and dihydrophthalides from celery. J. Org. Chem., 28, 985-987 (1963).
    • (1963) J. Org. Chem. , vol.28 , pp. 985-987
    • Gold, H.J.1    Wilson, C.W.2
  • 3
    • 0001322527 scopus 로고
    • Effect of phthalides on celery flavor
    • Uhlig, J. W., Chang, A., and Jen, J. J., Effect of phthalides on celery flavor. J. Food Sci., 52, 658-660 (1987).
    • (1987) J. Food Sci. , vol.52 , pp. 658-660
    • Uhlig, J.W.1    Chang, A.2    Jen, J.J.3
  • 4
    • 0344778751 scopus 로고
    • Volatile components of celery and celeriac
    • MacLeod, G., and Ames, J., Volatile components of celery and celeriac. Phytochem., 28, 1817-1824 (1989).
    • (1989) Phytochem. , vol.28 , pp. 1817-1824
    • MacLeod, G.1    Ames, J.2
  • 5
    • 0001204583 scopus 로고    scopus 로고
    • Stereoisomeric flavor compounds. 79. Simultaneous enantioselective analysis of 3-butylphthalide and 3-butylhexahydrophthalide stereoisomers in celery, celeriac, and fennel
    • Bartschat, D., Beck, T., and Mosandl, A., Stereoisomeric flavor compounds. 79. Simultaneous enantioselective analysis of 3-butylphthalide and 3-butylhexahydrophthalide stereoisomers in celery, celeriac, and fennel. J. Agric. Food Chem., 45, 4554-4557 (1997).
    • (1997) J. Agric. Food Chem. , vol.45 , pp. 4554-4557
    • Bartschat, D.1    Beck, T.2    Mosandl, A.3
  • 6
    • 0000977524 scopus 로고
    • Stimulation of glutathione S-transferase and inhibition of carcinogenesis in mice by celery seed oil constituents
    • American Chemical Society, Washington, DC
    • Zheng, G. Q., Zhang, J., Kenney, P. M., and Lam, L. K. T., Stimulation of glutathione S-transferase and inhibition of carcinogenesis in mice by celery seed oil constituents. In "ACS Symposium Series 546, Food Phytochemicals for Cancer Prevention 1," American Chemical Society, Washington, DC, pp. 230-238 (1994).
    • (1994) ACS Symposium Series 546, Food Phytochemicals for Cancer Prevention 1 , pp. 230-238
    • Zheng, G.Q.1    Zhang, J.2    Kenney, P.M.3    Lam, L.K.T.4
  • 7
    • 0035734603 scopus 로고    scopus 로고
    • Sedanolide, a natural phthalide from celery seed oil: Effect on hydrogen peroxide and tert-butyl hydroxyperoxide-induced toxicity in HepG2 and CaCo-2 human cell lines
    • Woods, J. A., Jewell, C., and O'Brien, N. M., Sedanolide, a natural phthalide from celery seed oil: effect on hydrogen peroxide and tert-butyl hydroxyperoxide-induced toxicity in HepG2 and CaCo-2 human cell lines. In Vitro and Molecular Toxicology, 14, 233-240 (2001).
    • (2001) In Vitro and Molecular Toxicology , vol.14 , pp. 233-240
    • Woods, J.A.1    Jewell, C.2    O'Brien, N.M.3
  • 8
    • 0035139052 scopus 로고    scopus 로고
    • Mosquitocidal, nematicidal, and antifungal compounds from Apium graveolens L. Seeds
    • Momin, R. A., and Nair, M. G., Mosquitocidal, nematicidal, and antifungal compounds from Apium graveolens L. Seeds. J. Agric. Food Chem., 49, 142-145 (2001).
    • (2001) J. Agric. Food Chem. , vol.49 , pp. 142-145
    • Momin, R.A.1    Nair, M.G.2
  • 9
    • 84989991267 scopus 로고
    • Terpene and sesquiterpene hydrocarbons in the essential oil from celery
    • Wilson, C. W., Terpene and sesquiterpene hydrocarbons in the essential oil from celery. J. Food Sci., 34, 521-523 (1969).
    • (1969) J. Food Sci. , vol.34 , pp. 521-523
    • Wilson, C.W.1
  • 10
    • 84989990401 scopus 로고
    • Identification and quantitative estimation of alcohols in essential oil
    • Wilson, C. W., Identification and quantitative estimation of alcohols in essential oil. J. Food Sci., 34, 535-537 (1969).
    • (1969) J. Food Sci. , vol.34 , pp. 535-537
    • Wilson, C.W.1
  • 11
    • 84986522816 scopus 로고
    • Relative recovery and identification of carbonyl compounds from celery essential oil
    • Wilson, C. W., Relative recovery and identification of carbonyl compounds from celery essential oil. J. Food Sci., 35, 765-768 (1970).
    • (1970) J. Food Sci. , vol.35 , pp. 765-768
    • Wilson, C.W.1
  • 12
    • 0001126647 scopus 로고
    • Free and glycosidically bound volatile compounds in fresh celery
    • Tang, J., Zhang, Y., Hartman, T. H., Rosen, R. T., and Ho, C.-T., Free and glycosidically bound volatile compounds in fresh celery. J. Agric. Food Chem., 38, 1937-1940 (1990).
    • (1990) J. Agric. Food Chem. , vol.38 , pp. 1937-1940
    • Tang, J.1    Zhang, Y.2    Hartman, T.H.3    Rosen, R.T.4    Ho, C.-T.5
  • 13
    • 0023612992 scopus 로고
    • Synthesis and absolute configuration of neocnidilide
    • Suzuki, H., Tanaka, A., and Yamashita, K., Synthesis and absolute configuration of neocnidilide. Agric. Biol. Chem., 51, 3369-3373 (1987).
    • (1987) Agric. Biol. Chem. , vol.51 , pp. 3369-3373
    • Suzuki, H.1    Tanaka, A.2    Yamashita, K.3
  • 14
    • 0025811535 scopus 로고
    • Pentacovalent oxaphosphorane chemistry in organic synthesis. 2. Total syntheses of (±)-trans- And (±)-cis-neocnidilides
    • McClue, C. K., and Jung, K.-Y., Pentacovalent oxaphosphorane chemistry in organic synthesis. 2. Total syntheses of (±)-trans- and (±)-cis-neocnidilides. J. Org. Chem., 56, 2326-2332 (1987).
    • (1987) J. Org. Chem. , vol.56 , pp. 2326-2332
    • McClue, C.K.1    Jung, K.-Y.2
  • 16
    • 2142814460 scopus 로고    scopus 로고
    • Solvent assisted flavour evaporation - A new and versatile technique for the careful and direct isolation of aroma compounds from complex food matrices
    • Engel, W., Bahr, W., and Schieberle, P., Solvent assisted flavour evaporation - a new and versatile technique for the careful and direct isolation of aroma compounds from complex food matrices. Eur. Food Res. Technol., 209, 237-241 (1999).
    • (1999) Eur. Food Res. Technol. , vol.209 , pp. 237-241
    • Engel, W.1    Bahr, W.2    Schieberle, P.3
  • 17
    • 34250103394 scopus 로고
    • Identification of the most intense volatile flavor compounds formed during autoxidation of linoleic acid
    • Ullrich, F., and Grosch, W., Identification of the most intense volatile flavor compounds formed during autoxidation of linoleic acid. Z. Lebensm. Unters. Forsch., 184, 277-282 (1987).
    • (1987) Z. Lebensm. Unters. Forsch. , vol.184 , pp. 277-282
    • Ullrich, F.1    Grosch, W.2
  • 20
    • 0000768506 scopus 로고
    • Natural occurrence of undecaenes in some fruits and vegetables
    • Berger, R. G., Drawert, F., Kollmannsberger, H., and Nits, S., Natural occurrence of undecaenes in some fruits and vegetables. J. Food Sci., 50, 1655-1656 (1985).
    • (1985) J. Food Sci. , vol.50 , pp. 1655-1656
    • Berger, R.G.1    Drawert, F.2    Kollmannsberger, H.3    Nits, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.