作者:Nagi Reddy Modugu、Jagadeshwar Vannada、Goverdhan Mehta
DOI:10.1016/j.tetlet.2015.11.001
日期:2015.12
synthetic approach towards kinamycins that harnesses the proclivities of the norbornyl scaffold is unveiled to access the oxy-functionalized and actively side-armed cyclohexenoid ring-D of these bioactive natural products. This ring-D building block has been further elaborated to the tricyclic ABD ring system present in kinamycins.
揭示了一种利用降冰片基支架的倾向性的对那那霉素的合成方法,以接近这些生物活性天然产物的经氧官能化并带有侧链的活跃的环己烯酮环D。这种环D的构建基块已被进一步精细化为存在于那那霉素中的三环ABD环系统。