Acta Chimica Sinica ›› 1990, Vol. 48 ›› Issue (3): 307-311. Previous Articles     Next Articles

Original Articles

一种选择性去三苯甲基保护基的方法

孙快麟;李润荪;雷兴翰   

  1. 国家医药管理局上海医药工业研究院
  • 发布日期:1990-03-15

A mild and selevtive method of detritylation

SUN KUAILIN;LI RUNSUN;LEI XINGHAN   

  • Published:1990-03-15

A method of mild and selective detritylation is reported. The sugar derivatives with a variety of protective groups, were detritylated with 4-MeC6H4SO3H (0.1-0.2 equivalent) in CH2Cl2 at room temperature Acid sensitive groups such as isopropylidene, methoxylmethyl (MOM), methoxyl ethoxyl Me (MEM), tert-butyldimethylsilyl (TBDMS), and glycosidic benzoyl survived. With pentose derivatives containing two trityls at 1-, 5-position, 1-trityloxy can be cleaved selectively at lower reaction temperature and shorter reaction time,. Yields range from 53 to 90%.

Key words: SELECTIVITY, GLUCOSE, FURANOSE, REMOVAL, TRIPHENYLMETHANE, PROTECTIVE GROUP

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