作者:Ana R. Rodriguez、Bernd W. Spur
DOI:10.1016/j.tetlet.2012.10.059
日期:2012.12
The total synthesis of Resolvin D1, a potent endogenous anti-inflammatory lipid mediator derived from docosahexaenoic acid, has been achieved. The chiral hydroxy-groups at C7, C8 and C17 were obtained via a chiral pool strategy from 2-deoxy-d-ribose. Wittig reactions followed by a modified Pd0/CuI Sonogashira coupling and Zn(Cu/Ag) cis-reduction completed the total synthesis of Resolvin D1.
已经实现了Resolvin D1的全合成,Resolvin D1是一种有效的内源性二十二碳六烯酸衍生的抗炎脂质介体。通过手性池策略从2-脱氧-d-核糖获得C7,C8和C17处的手性羟基。Wittig反应,然后进行修饰的Pd 0 / Cu I Sonogashira偶联和Zn(Cu / Ag)顺式还原,完成了Resolvin D1的总合成。