[1]李雯,刘宏民,张霞..对位取代苯酚葡萄糖氧甙类化合物红外光谱特征[J].郑州大学学报(工学版),1999,20(04):41-43.[doi:10.3969/j.issn.1671-6833.1999.04.013]
　LI Wen,LIU Hongmin,Zhang Xia.Infrared spectral characteristics of para-substituted phenol glucosoxyglycosides[J].Journal of Zhengzhou University (Engineering Science),1999,20(04):41-43.[doi:10.3969/j.issn.1671-6833.1999.04.013]
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对位取代苯酚葡萄糖氧甙类化合物红外光谱特征()
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《郑州大学学报(工学版)》[ISSN:1671-6833/CN:41-1339/T]

卷:
20
期数:
1999年04期
页码:
41-43
栏目:
出版日期:
1999-01-01

文章信息/Info

Title:
Infrared spectral characteristics of para-substituted phenol glucosoxyglycosides
作者:
李雯; 刘宏民; 张霞.
郑州工业大学化工学院,河南,郑州,450002, 郑州大学化学化工学院,河南,郑州,450052, 河南省医药学校,河南,开封,475001
Author(s):
LI Wen; LIU Hongmin; Zhang Xia
关键词:
对位取代苯酚;  葡萄糖甙;  红外光谱
Keywords:
DOI:
10.3969/j.issn.1671-6833.1999.04.013
文献标志码:
A
摘要:
在对位取代苯酚葡萄糖甙类化合物结构与活性关系的研究过程中,发现了强烈抑制端粒酶活性的化合物.此类化合物经西德PE-1710型红外光谱仪测得红外光谱吸收表明,其C-O键、葡萄糖吡喃环及笨环的吸收呈现明显的红外光谱特征,即随化合物电负性的规律性变化,其红外光谱吸收也呈现规律性变化.此外,进一步讨论了C1-H核磁共振位移与葡萄糖吡喃环红外吸收峰的关系.迄今尚未发现类似的研究报道.
Abstract:
In the study of the relationship between structure and activity of para-substituted phenol glucosides, compounds that strongly inhibit telomerase activity were found. The infrared spectral absorption of such compounds measured by the West German PE-1710 infrared spectrometer showed that the absorption of C-O bonds, glucose pyran rings and ben rings showed obvious infrared spectral characteristics, that is, with the regular change of electronegativity of the compounds, the infrared spectral absorption also showed regular changes. In addition, the relationship between C1-H NMR displacement and glucose pyran ring infrared absorption peak is further discussed. No similar studies have been reported to date.

更新日期/Last Update: 1900-01-01