吲哚
化学
糖基化
吲哚试验
核苷
催化作用
溶剂
立体化学
组合化学
有机化学
生物化学
作者
Martin Humeník,Peter Kutschy,Vladimı́r Kováčik,Slávka Bekešová
出处
期刊:ChemPlusChem
[Institute of Organic Chemistry & Biochemistry, Academy of Sciences of the Czech Republic]
日期:2005-01-01
卷期号:70 (4): 487-506
被引量:7
摘要
A convergent synthesis of 1-(β-D-glucopyranosyl)-, 1-(α-D-mannopyranosyl)- and 1-(β-D-ribofuranosyl)benzocamalexin was elaborated as an alternative route to the linear approach based on the indoline-indole method. 1,2-Anhydrosaccharides and 1,2-cyclic sulfites as saccharide donors were used in the key glycosylation step. Coupling with benzocamalexin resulted in moderate to excellent yields of nucleoside analogs, depending on the saccharide donor, catalyst and solvent used.
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