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Analysis of the linkage positions and isomers of monosaccharide units in oligosaccharides by negative secondary ion mass spectrometry in combination with the stereoselective reaction with substituted boronic acid

Analysis of the linkage positions and isomers of monosaccharide units in oligosaccharides by negative secondary ion mass spectrometry in combination with the stereoselective reaction with substituted boronic acid

作     者:YAN,Lin FANG,Yi-Wei Institute of Chemistry,Chinese Academy of Sciences,Beijing 100080 

作者机构:Institute of Chemistry Chinese Academy of Sciences Beijing 100080 

出 版 物:《Chinese Journal of Chemistry》 (中国化学(英文版))

年 卷 期:1993年第11卷第1期

页      面:53-58页

核心收录:

学科分类:07[理学] 0703[理学-化学] 

基  金:Project supported by the National Natural Science Foundation of China 

主  题:Analysis of the linkage positions and isomers of monosaccharide units in oligosaccharides by negative secondary ion mass spectrometry in combination with the stereoselective reaction with substituted boronic acid acid 

摘      要:The negative secondary ion mass spectrometry,in combination with the stereoselective derivatizations with substituted boronic acid RB(OH)_2,was used in the analysis of fourteen oligosac- *** mass spectra of the derivatives provide information on their linkage Positions and iso- merism of the individual monoscaccharide *** results indicated that among the derivatives of the oligosaccharides analyzed,those with 1—4 and 1—6 linkages all presented the ion peaks at m/z 287,sometimes one more peak at m/z ***,a relationship was found between the linkage positions and the intensity orders of the derivative ***,the derivatives of the disaccharides with a galactose presented an intense ion peak at m/z 347,and those of oligosaccharides with 1—6 linkage to a galactose at terminal presented the ion at m/z *** the case of oligosaccharides with a fructose residue,characteristic ion of m/z 155 was *** conditions of stereoselective derivatizations and mass spectrometry were studied,in order to obtain a better reproducibility of the mass spectra.

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