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本文利用了多种NMR技术,其中包括1H 13C NMR,DEPT、COSY、C,H-COSY、COLOC和NOE差谱,首次确定了圆果皂甙元的结构及构型。 相似文献
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苯并二氢呋喃类木脂素NMR谱的研究 总被引:3,自引:1,他引:2
用2D NMR技术研究了从水飞蓟素中分离的一个苯并二氢呋喃类木脂素的结构,证实该类化合物的取代基位置可用COLOC谱确定。同时研究了该类化合物以DMSO-d6为溶剂的PMR谱的特征,另外对Balanophonin的PMR谱进行了详细归属。 相似文献
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Enzymatic catalysis of 2,6-dimethoxyphenol by laccases and products characterization in organic solutions 总被引:1,自引:0,他引:1
2,6-Dimethoxyphenol (DMP) as a substrate was widely used in determination of laccase activity. It is surprising, however, that its catalyzed oxidation products have not been completely determined until now. Studies were thus conducted on Rhus laccase (RL) and immobilized Rhus laccase (IRL)-catalyzed oxidation reactions of 2,6-dimethoxyphenol in water-organic solvent systems. These reactions pro- ceeded well in water-(im)miscible organic solvent systems pre-saturated with water. Only one product, 3,3′,5,5′-tetramethoxy-1,1′biphenyl-4,4′-diol (TMBP), was produced by RL catalysis, and it was thor- oughly characterized by FT-IR, NMR, GC-MS, etc. A simple enzymatic mechanism of this reaction is proposed. 相似文献
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应用1H-1H COSY,13C-1H COSY及COLOC并结合其它波谱技术对从中药白花前胡(Peucedanum praeruptorum Dunn)根中分得的一种新化合物前胡香豆素F进行了深入研究,其化学结构确定为3'-异戍烯酰氧基花椒内酯,为吡喃环上3'位烯醇羟基的氧原子和异戍烯酰基形成的烯醇酯.这种新颖结构在自然界中比较少见。 相似文献
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Complete 1H and 13C spectral assignments of 17beta- and 17alpha-hydroxy epimers of three biologically active sterols (boldenone, 3-methoxyestradiol and 3-methoxydihydroequilenin) were achieved making use of one- and two-dimensional NMR techniques (1D-HOHAHA, DEPT, COSY, NOESY, TOCSY, HSQC and COLOC). 相似文献
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1H and13C NMR spectra of 7-diethylamino-4-(1,2,3-triazol-1-yl)-2H-1-benzopyran-2-one derivatives have been studied. The location of the substituent in the 1,2,3-triazole ring was determined by the 2D COLOC method. It was established that the H(3) and H(5) protons in the coumarin moiety experience anisotropic influence of the phenyl subsituent at the C(5) atom in the triazole ring.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1330–1332, July, 1994. 相似文献
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Joseph K. Rugutt Nikolaus H. Fischer Marcus A. Nauman Thomas J. Schmidt Dana K. Berner 《光谱学快报》2013,46(4):711-726
The high field 1H and 13C resonances of obacunone were established by a series of I D and 2D NMR experiments. The 13C-NMR signals of the five tertiary methyl groups and all quatenary carbons were unambiguously assigned. The results confirm the stereochemical assignments at all stereogenic centres. 相似文献