首页> 外文期刊>Chemistry Letters >Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride Having Phthaloyl or Dichlorophthaloyl Protected Amino Function Using a 1:2 Combination of Stannic Chloride and Silver Tetrakis(pentafluorophenyl)borate
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Catalytic and Stereoselective Glycosylation with Disarmed Glycosyl Fluoride Having Phthaloyl or Dichlorophthaloyl Protected Amino Function Using a 1:2 Combination of Stannic Chloride and Silver Tetrakis(pentafluorophenyl)borate

机译:锡烷基锡与四(五氟苯基)硼酸银的1:2组合使用具有邻苯二甲酰基或二氯邻苯二甲酰基保护的氨基官能团的脱甲糖基氟化物催化和立体选择性糖基化

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摘要

A catalytic and stereoselective glycosylation of various glycosyl acceptors with disarmed glycosyl fluorides having phthaloyl or dichlorophthaloyl rpotected amino function is successfully carried out by tetrakis(pentafluorophenyl)borate [AgB(C_6F_5)_4] in the coexistence of MS 5A, and the corresponding 1,2-trans disaccharides are obtained in high yields.
机译:通过四(五氟苯基)硼酸盐[AgB(C_6F_5)_4]与MS 5A共存,并且相应的1,2,成功地通过具有邻苯二甲酰基或二氯邻苯二甲酰基的氨基官能团的解除武装的糖基氟化物对各种糖基受体进行催化和立体选择性糖基化反式二糖以高产率获得。

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