作者:Jeannette T. Bowler、Caitlin R. Clausen、Daniel J. Blackburn、Weiming Wu
DOI:10.1016/j.tetlet.2014.10.005
日期:2014.11
A convenient and efficient method for the synthesis of N1-substituted orotic acid derivatives is reported. The synthetic route utilizes substituted maleimide as synthetic intermediate and takes only four simple steps from readily available starting materials. As a result, orotic acid derivatives with various alkyl and aromatic groups at N1 can be readily synthesized.
报道了一种方便有效的合成N 1-取代的乳清酸衍生物的方法。合成路线利用取代的马来酰亚胺作为合成中间体,并且从容易获得的起始原料开始仅需四个简单步骤。结果,可以容易地合成在N1处具有各种烷基和芳族基团的乳清酸衍生物。