Rapid O-glycosidation of phenols with glycosyl fluoride by using the combinational activator, Cp2HfCl2-AgClO4

Rapid O-glycosidation of phenols with glycosyl fluoride by using the combinational activator, Cp2HfCl2-AgClO4
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使用组合活化剂 Cp2HfCl2-AgClO4 使苯酚与糖基氟发生快速 O-糖苷化

DOI:
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发表时间:
1989
期刊:
影响因子:
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通讯作者:
Keisuke Suzuki
Keisuke Suzuki
中科院分区:
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文献类型:
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作者:
Takashi Matsumoto;M. Katsuki;Keisuke Suzuki

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介绍了一种新的有效的苯酚O-糖苷化方法。在4A分子筛存在下,Cp2HfCl2-AgClO4是糖基氟化物和苯酚偶联反应的高效促进剂,该反应在低温下快速进行,高产率地生成O-芳基糖苷。
A new and efficient method for O-glycosidation of phenols is described. Cp2HfCl2–AgClO4 is a highly effective promoter for the coupling reaction between glycosyl fluoride and phenol in the presence of molecular sieves 4A, which proceeds rapidly at low temperature to give O-aryl glycoside in high yields.