The present invention relates the asymmetrical synthesis of heterocyclic compounds of pharmaceutical interest. In particular a series of enantioselective methods is described, allowing the synthesis and transformations of isoindolinones of Formula (I), into high yields and enantiomeric excesses >90%.
本发明涉及对药用异戊二
酮类化合物的不对称合成。具体而言,描述了一系列具有对映选择性的方法,允许将式(I)的异
戊二酮进行合成和转化,产率高且对映过量大于90%。