化学
选择性
路易斯酸
二醇
高效液相色谱法
色谱法
柱色谱法
氮气
有机化学
催化作用
作者
Robin Tuytten,Filip Lemière,Eddy L. Esmans,Wouter Herrebout,Benjamin J. van der Veken,Bert U. W. Maes,Erwin Witters,Russell P. Newton,Ed Dudley
摘要
Urinary modified nucleosides have a potential role as cancer biomarkers, and most of the methods used in their study have utilized low-pressure phenylboronate affinity chromatography materials for the purification of the cis-diol-containing nucleosides. In this study, a boronate HPLC column was surprisingly shown not to trap the nucleosides as would be expected from experience with the classic Affigel 601 resin but showed only partial selectivity toward cis-diol groups while other groups exhibited better retention. In aprotic conditions, trapping of nucleosides was possible; however, the selectivity toward cis-diol-containing compounds was lost with the Lewis basicity of available nitrogens being the main determinant of retention. The experimental findings are compared to and confirmed by DFT calculations.
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