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NUCLEAR MAGNETIC RESONANCE SPECTROSCOPIC ANALYSIS OF HOMOALLYLIC AND BIS HOMOALLYLIC SUBSTITUTED METHYL FATTY ESTER DERIVATIVES

机译:同质和双异质取代甲基脂肪酯衍生物的核磁共振谱分析

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摘要

Using a combination of selective irradiation H-1 nuclear magnetic resonance experiments and two-dimensional (HC)-H-1-C-13 correlation spectroscopy spectral analysis of homoallylic and bis homoallylic substituted (azido, acetoxy, chloro and oxo) fatty ester derivatives, the carbon shifts of the ethylenic carbon atoms were determined. In the case of methyl 12-azido-9Z-octadecenoate (homoallylic), the carbon chemical shifts of the ethylenic C-9 and C-10 carbon nuclei are 133.092 and 124.596 ppm, respectively. In methyl 9-azido-12Z-octadecenoate (bis homoallylic), the carbon chemical shift of the ethylenic C-12 and C-13 carbon nuclei are 128.118 and 131.243 ppm, respectively. [References: 19]
机译:结合使用选择性辐射H-1核磁共振实验和二维(HC)-H-1-C-13相关光谱法对均烯丙基和双均烯丙基取代的(叠氮基,乙酰氧基,氯代和氧代)脂肪酯衍生物进行光谱分析,确定了烯属碳原子的碳位移。对于12-叠氮基-9Z-十八烯酸甲酯(均烯丙基)而言,烯键式C-9和C-10碳核的碳化学位移分别为133.092和124.596 ppm。在9-叠氮基-12Z-十八烯酸甲酯(双均烯丙基)中,烯键式C-12和C-13碳核的碳化学位移分别为128.118 ppm和131.243 ppm。 [参考:19]

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