The structure–activity relationship of the unusual indolosesquiterpenoid mycoleptodiscin A is unknown due to natural scarcity and inefficient synthesis. A modular approach leveraging Larock indole synthesis has been established to access mycoleptodiscin A and a divergent collection of drimenyl indoles. It features the utilization of an inexpensive (+)-sclareolide, modularity, purification-economy,
由于自然稀缺性和合成效率低下,不常见的
吲哚半
萜类霉霉盘素 A 的结构-活性关系尚不清楚。已经建立了利用 Larock
吲哚合成的模块化方法来获取支菌素 A 和不同的连苯酰
吲哚集合。它的特点是利用廉价的 (+)-
香紫苏内酯、模块化、纯化经济性和可扩展性,这有助于对支菌素 A 和相关前体的首次
生物学评估。