Total synthesis of 6-deoxyclitoriacetal isolated from Stemona collinsae Craib.
作者:Prapas Khorphueng、Jumreang Tummatorn、Amorn Petsom、Richard J.K. Taylor、Sophon Roengsumran
DOI:10.1016/j.tetlet.2006.05.188
日期:2006.8
A total synthesis of the rotenoid, 6-deoxyclitoriacetal, a cytotoxic natural product, was successfully achieved by using platinum-catalysed hydroarylation, Sharpless asymmetric dihydroxylation, regioselective IBX diol oxidation and stereoselective intramolecular keto-aldehyde pinacol coupling as the key steps.
通过使用铂催化的氢芳基化,Sharpless不对称二羟基化,区域选择性IBX二醇氧化和立体选择性分子内酮-醛频哪醇偶联作为关键步骤,成功地完成了类胡萝卜素6-脱氧clicercercetal的全合成,这是一种细胞毒性天然产物。