作者:Hiroshi Osato、Ian L. Jones、Huini Goh、Christina L.L. Chai、Anqi Chen
DOI:10.1016/j.tetlet.2011.09.035
日期:2011.11
A three-step, one-pot process has been developed for the synthesis of 5-epi-shikimic acid derivative 5 using inexpensive and abundant d-ribose as the starting material. Based on this pivotal intermediate, the syntheses of two key shikimic acid derivatives 6 and 7 for Tamiflu have been achieved in a concise and practical fashion.
已经开发了一种三步一锅法,以廉价且丰富的d-核糖为起始原料合成5-表-ki草酸衍生物5。基于这一关键中间体,以简洁实用的方式实现了达菲的两种关键sh草酸衍生物6和7的合成。