作者:Adusumilli Srikrishna、Gedu Satyanarayana
DOI:10.1016/j.tetasy.2005.11.012
日期:2005.12
An enantiospecific total synthesis of patchouli alcohol, starting from the readily available monoterpene (R)-carvone, has been accomplished. A tandem double Michael reaction–alkylation sequence and single electron mediated 6-endo trig cyclisation reaction have been employed as key steps.
从容易获得的单萜(R)-香芹酮开始,完成了广patch香醇的对映体特异性全合成。串联的双迈克尔反应-烷基化序列和单电子介导的6-内基Trig环化反应已被用作关键步骤。