Isolation of the Major Phenolic Compounds in the Pits of Brined Green Olive Drupes: Structure Elucidation by Comprehensive 1H/13C-NMR Spectroscopy

被引:6
|
作者
Khallouki, Farid [1 ,2 ,3 ]
Hull, William E. [4 ]
Wuertele, Gerd [1 ,2 ]
Haubner, Roswitha [1 ,2 ]
Erben, Gerhard [4 ]
Owen, Robert W. [1 ,2 ]
机构
[1] Natl Ctr Tumor Dis, Div Prevent Oncol, Neuenheimer Feld 460, Heidelberg, Germany
[2] German Canc Res Ctr, Div Prevent Oncol, Heidelberg, Germany
[3] Fac Sci & Tech, Team Physiol Pharmacol & Endocrinol, Errachidia, Morocco
[4] German Canc Res Ctr, Core Facil Mol Struct Anal, Heidelberg, Germany
关键词
Antioxidants; HPLC; mass spectrometry; Mediterranean diet; C-13-NMR; H-1-NMR; olive pits; phenolic compounds; olive mill waste products; LIGNANS; OIL; CONSTITUENTS; SECOIRIDOIDS; NUZHENIDE; FRUITS; SEED;
D O I
10.1177/1934578X19857365
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pits of representative green olive drupes from Italy and Greece were evaluated for their content of phenolic compounds. The major purified polyphenols quantitated in mg/kg in the Italian and Greek pit varieties, respectively, were tyrosol (157 and 523), hydroxytyrosol (3 386 and 1723), vanillin (151 and 83), vanillic acid (58 and 101), phloretic acid (85 and 0), (+)-pinoresinol (954 and 877), (+)-1-acetoxypinoresinol (114 and 105), dehydrodiconiferyl alcohol (340 and 386) and the corresponding aldehyde (398 and 553), the erythro and threo isomers of guaiacylglycerol-beta-coniferol ether (78 and 147) and (93 and 273) and their corresponding aldehydes (238 and 349) and (232 and 537), and finally nuzhenide (186 and 364). The data indicate that the waste products of olive mills should be a rich source of a variety of polyphenolic compounds. Detailed H-1- and C-13-nuclear magnetic resonance data are presented, representing the most comprehensive and unambiguous results available to date for the compounds studied.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Structure of binuclear platinum(III) acetamidate complexes in solutions as probed by 195Pt, 13C, and 1H NMR spectroscopy
    Kirakosyan, G. A.
    Fedotova, T. N.
    Kuznetsova, G. N.
    RUSSIAN CHEMICAL BULLETIN, 2015, 64 (10) : 2408 - 2414
  • [42] The structural and dynamic properties of 1-bromodecane in urea inclusion compounds investigated by solid-state 1H, 13C and 2H NMR spectroscopy
    Yang, Xiaorong
    Mueller, Klaus
    MAGNETIC RESONANCE IN CHEMISTRY, 2011, 49 (08) : 514 - 522
  • [43] The discovery-oriented approach to organic chemistry -: 1.: Nitration of unknown organic compounds -: An exercise in 1H NMR and 13C NMR spectroscopy for sophomore organic laboratories
    McElveen, SR
    Gavardinas, K
    Stamberger, JA
    Mohan, RS
    JOURNAL OF CHEMICAL EDUCATION, 1999, 76 (04) : 535 - 536
  • [44] Structure elucidation and assignment of 1H and 13C spectra of the new fused cyclobutane-naphthofuran derivative by two-dimensional NMR in different solvents
    Cvijin, IV
    Marinic, Z
    Sindler-Kulyk, M
    SPECTROSCOPY LETTERS, 1998, 31 (05) : 989 - 1000
  • [45] Geometry and halogen regiochemistry determination of vicinal vinyl dihalides by 1H and 13C NMR.: Application to the structure elucidation of prefuroplocamioid, an unusual marine monoterpene
    Díaz-Marrero, AR
    Cueto, M
    Dorta, E
    Rovirosa, J
    San-Martín, A
    Darias, J
    ORGANIC LETTERS, 2002, 4 (17) : 2949 - 2952
  • [46] (3,2)D 1H, 13C BIRDr,X-HSQC-TOCSY for NMR structure elucidation of mixtures: application to complex carbohydrates
    Brodaczewska, Natalia
    Kostalova, Zuzana
    Uhrin, Dusan
    JOURNAL OF BIOMOLECULAR NMR, 2018, 70 (02) : 115 - 122
  • [47] Sequential assignment of 1H, 15N, 13C resonances and secondary structure of human calmodulinlike protein determined by NMR spectroscopy
    Qian, H
    Rogers, MS
    Schleucher, J
    Edlund, U
    Strehler, EE
    Sethson, I
    PROTEIN SCIENCE, 1998, 7 (11) : 2421 - 2430
  • [48] Determination of C-23 Configuration in (20R)-23-Hydroxycholestane Side Chain of Steroid Compounds by 1H and 13C NMR Spectroscopy
    Kicha, Alla A.
    Kalinovsky, Anatoly I.
    Antonov, Alexander S.
    Radchenko, Oleg S.
    Ivanchina, Natalia V.
    Malyarenko, Timofey V.
    Savchenko, Alexander M.
    Stonik, Valentin A.
    NATURAL PRODUCT COMMUNICATIONS, 2013, 8 (09) : 1219 - 1222
  • [49] Structure elucidation, total assignment of the 1H and 13C chemical shifts, and absolute configuration by NMR techniques of dammarane-type triterpenes from Hippocratea volubilis
    Kennedy, Maria L.
    Lopez-Arencibia, Atteneri
    Reyes-Batlle, Maria
    Lorenzo-Morales, Jacob
    Pinero, Jose E.
    Bazzocchi, Isabel L.
    Jimenez, Ignacio A.
    MAGNETIC RESONANCE IN CHEMISTRY, 2018, 56 (01) : 46 - 54
  • [50] Simultaneous analysis of the oxidation of solvent-extracted and cold-pressed green coffee oil during accelerated storage using 1H NMR and 13C NMR spectroscopy
    Dong, Wenjiang
    Hong, Qidi
    Cheng, Jinhuan
    He, Hongyan
    Li, Yanan
    Hu, Rongsuo
    Long, Yuzhou
    FOOD RESEARCH INTERNATIONAL, 2023, 165