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      核磁共振     
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  nmr
    Solid State NMR Study of Methanol Conversion Reaction
    甲醇催化转化反应的固体核磁共振研究
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    Applications of High Resolution Liquid State NMR Spectroscopy in Surfactant Chemistry and Neurochemistry
    液体高分辨核磁共振波谱在表面活性剂化学和神经化学研究中的应用
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    NMR Study of Some Substituted Benzothiazepines——(Ⅰ)~1H NMR Spectra
    氢化苯骈硫氮杂核磁共振谱的研究 Ⅰ、~1H 核磁共振
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    ~(13)C NMR SPECTROSCOPIC STUDIES OF SEVERAL NEW DITERPENOID ALKALOIDS FROM ACONITUM SPECIES
    几个新乌头碱型——二萜生物碱的~(13)C核磁共振谱研究
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    STUDY ON THE INTERACTION OF CISPLATIN WITH NUCLEOSIDES BY ~(13)C NMR
    顺式二氯二氨合铂与核苷作用的~(13)C核磁共振研究
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  nuclear magnetic resonance
    ANALYSIS OF NUCLEAR MAGNETIC RESONANCE SPECTRA IN 2-CHLORO-6-TRICHLOROMETHYL PYRIDINE
    2-氯-6-(三氯甲基)吡啶核磁共振谱的解析
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    Nuclear Magnetic Resonance Study of Some Substituted Benzothiazepines——Ⅱ.~(13)C Nuclear Magnetic Resonance Spectra
    氢化苯骈硫氮杂(艹卓)核磁共振谱的研究 Ⅱ、~(13)C核磁共振
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    ~(13)C Nuclear Magnetic Resonance of Diterpenoid Alkaloids
    二萜生物碱的~(13)C核磁共振
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    DETERMINATION OF GARAMINE PK_a BY CARBON-13 NUCLEAR MAGNETIC RESONANCE
    用碳-13核磁共振法测定加纳霉胺的Pk_a值
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    Nuclear Magnetic Resonance Studies on Metal Ion Complexes of cAMP and its Derivatives
    cAMP及其衍生物金属离子铬合物的核磁共振研究
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  nmr spectroscopy
    Applications of High Resolution Liquid State NMR Spectroscopy in Surfactant Chemistry and Neurochemistry
    液体高分辨核磁共振波谱在表面活性剂化学和神经化学研究中的应用
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    ~(13)C NMR Spectroscopy of Some Fluoro-containing Unsaturated Esters
    含氟不饱和酯的~(13)C核磁共振
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    STUDIES ON STRUCTURE AND SYNTHESIS OF ARTEANNUIN AND RELATED COMPOUNDS Ⅷ. DETERMINATION OF CONFIGURATION OF ARTEANNUIN DEGRADATION PRODUCTS AND RELATED COMPOUNDS BY ~1H NMR SPECTROSCOPY
    青蒿素及其类似物的结构和合成 Ⅷ、~1H核磁共振测定青蒿素降解物及有关化合物的构型
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    EXAMPLES OF ~(31)P NMR SPECTROSCOPY APPLICATION
    ~(31)P核磁共振谱应用数则
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    NMR SPECTROSCOPY STUDIES OF HUMIC ACID——The T_1 values and the relative contents of various types of carbons in methylated humic acids
    腐植酸核磁共振波谱的研究——几种甲基化腐植酸中各类碳的T_1值和相对含量
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  nmr spectra
    NMR Study of Some Substituted Benzothiazepines——(Ⅰ)~1H NMR Spectra
    氢化苯骈硫氮杂核磁共振谱的研究 Ⅰ、~1H 核磁共振
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    ORGANOTITANIUM CHEMISTRY Ⅳ.~(13)C NMR SPECTRA OF TITANOCENE DICHLORIDES DERIVATIVES
    有机钛化学——Ⅳ.二氯二取代茂钛衍生物的~(13)C核磁共振
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    NMR SPECTRA OF RANDOM BUTADIENESTYRENE COPOLYMER PEAK ASSIGNMENT OF CARBON-13 NMR SPECTRA
    无规丁苯共聚物的核磁共振波谱——~(13)C-NMR谱带的归属
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    Studies on Organolanthanide Complexes ⅩⅨ.1~H and (13)~C NMR Spectra of Dicyclopentadienyl Y and Lu Chlorides
    镧系金属有机配合物的研究——ⅩⅠⅩ.二茂型氯化钇和镥的~1H和~(13)C核磁共振
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    Synthesis, Identification and Assignments of the NMR Spectra of 1,2,4, 6-tetraarylpyridinium Perchlorates
    1,2,4,6,-四芳环呲啶鎓高氯酸盐的合成及其核磁共振谱的解析
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  nmr
       On the basis of total acid hydrolysis, methylation analysis, periodate oxidation and NMR studies (1H and 13C) the structure of the repeating unit of the polysaccharide was assigned and indicated only α-(1→4) linked Glucan.
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       The stereo-structures of Roridin P and Isororidin P were established on the basis of one- and two-dimensional nuclear magnetic resonance (NMR) spectral analyses.
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       The aim of this study was to synthesize and identify 2,4-dihalogenofluorobenzene (or trihalogenobenzene) derivatives by spectroscopic means, 1H-NMR and 19F-NMR.
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       The synthesized compounds have been characterized on the basis of elemental analyses, infrared spectroscopy (IR), and nuclear magnetic resonance (NMR).
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       Two compounds were designed, synthesized, and characterized by 1H-nuclear magnetic resonance (1H-NMR), ultraviolet (UV)-visible, and matrix-assisted laser desorption/ionization (MALDI) mass spectra.
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  nuclear magnetic resonance
       The stereo-structures of Roridin P and Isororidin P were established on the basis of one- and two-dimensional nuclear magnetic resonance (NMR) spectral analyses.
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       The synthesized compounds have been characterized on the basis of elemental analyses, infrared spectroscopy (IR), and nuclear magnetic resonance (NMR).
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       Two compounds were designed, synthesized, and characterized by 1H-nuclear magnetic resonance (1H-NMR), ultraviolet (UV)-visible, and matrix-assisted laser desorption/ionization (MALDI) mass spectra.
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       Both monomers and polymers were characterized by Fourier transform infrared spectroscopy, 1H nuclear magnetic resonance, and elemental analysis measurements, and their structures were identified.
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       Their structures were identified by nuclear magnetic resonance and mass spectrum.
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  nmr spectroscopy
       1H-NMR spectroscopy and pattern recognition (PR) method were used to assess the acute biochemical effects of light rare earths.
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       Correct synthesis and folding were confirmed by MALDI-TOF mass spectrometry and NMR spectroscopy, respectively.
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       Derivatives of MEC were found by 1H-NMR spectroscopy under stress conditions in colorless mutants of the bacteria and isolated to be subsequently purified and used for modulation of the immune system of animals.
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       13C-NMR spectroscopy revealed both polysaccharides to be linear partially acetylated 1,4-β-D-glucomannans.
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       Chemical analysis and 13C-NMR spectroscopy revealed the presence of D-mannopyranose and D-glucopyranose in the heteropolysaccharide at a molar ratio of 1.39 : 1.
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  nmr spectra
       Each NMR spectra was data-processed to provide 238 intensity-related descriptors as input coordinates in a multidimensional space and analyzed by PR method.
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       Many low-molecular weight metabolites were identified by 1H-NMR spectra of the rat serum.
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       The structure of the polymer was confirmed by 1H-NMR spectra.
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       Their chemical structures were determined to show trans-vinylene character according to infrared (IR) and 1H nuclear magnetic resonance (NMR) spectra.
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       13C NMR spectra of both fractions were identical with respect to the number and positions of signals, which indicates that their primary structures were identical.
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