作者:Adrián Covarrubias-Zúñiga、Armando Gonzalez-Lucas、Mireya M. Domı́nguez
DOI:10.1016/s0040-4020(03)00102-9
日期:2003.3
convergent total synthesis of the natural compound mycophenolic acid 1 is described. The synthetic strategy for the construction of the hexasubstituted aromatic nucleus was based on a ring annulation sequence, involving a Michael addition reaction and intramolecular Dieckmann condensation reaction in situ as the key step. Subsequent transformations of the substituents afforded the target mycophenolic acid
描述了天然化合物霉酚酸1的收敛的全合成。构建六取代芳族核的合成策略是基于环环化序列,其中包括迈克尔加成反应和分子内狄克曼缩合原位反应为关键步骤。取代基的随后转化提供了目标麦考酚酸1。