An enantiospecific synthesis of (−)-2-pupukeanone via a rhodium carbenoid CH insertion reaction
作者:A Srikrishna、P Ravi Kumar、Santosh J Gharpure
DOI:10.1016/s0040-4039(01)00585-8
日期:2001.6
An enantiospecific synthesis of (−)-2-pupukeanone, starting from (R)-carvone employing a Michael–Michael reaction and an intramolecular rhodium carbenoid CH insertion reaction as the key steps for the generation of the isotwistane framework, is described.
描述了从(R)-香芹酮开始的对映体特异性合成(-)-2-pupukeanone的过程,该反应采用Michael-Michael反应和分子内铑类胡萝卜素CH插入反应作为生成异twistane骨架的关键步骤。