Synthesis of indolo[2,3-a]carbazole glycoside analogs of rebeccamycin: inhibitors of cyclin D1-CDK4
作者:Margaret M. Faul,、Kevin A. Sullivan、John L. Grutsch、Leonard L. Winneroski、Chuan Shih、Concha Sanchez-Martinez、Jeremy T. Cooper
DOI:10.1016/j.tetlet.2003.10.184
日期:2004.1
The synthesis and structure–activity relationships of a new series of indolo[2,3-a]carbazole glycosides, analogs of rebeccamycin, derived from the natural sugars (glucose, fucose, mannose, xylose, rhamnose, and galactose) is described.
描述了从天然糖(葡萄糖,岩藻糖,甘露糖,木糖,鼠李糖和半乳糖)衍生的新系列吲哚[2,3- a ]咔唑糖苷(瑞贝卡霉素类似物)的合成与构效关系。