作者:A. Srikrishna、G. Satyanarayana
DOI:10.1016/j.tet.2005.07.016
日期:2005.9
A formal total synthesis of the marine sesquiterpene (±)-9-isocyanoneopupukeanane starting from the readily available monoterpene carvone has been accomplished employing a combination of intermolecular Michael addition–intramolecular Michael addition reaction and an intramolecular rhodium carbenoid C–H insertion reaction as key steps, and identifying the isopropenyl group as a masked hydroxy group.
从分子间迈克尔加成-分子间迈克尔加成反应和分子内铑类胡萝卜素C-H插入反应作为关键步骤,已经完成了从容易获得的单萜香芹酮开始的海洋倍半萜烯(±)-9-异氰酮-opukekeanane的正式全合成。 ,并将异丙烯基标识为被掩盖的羟基。